The following pages link to Template:Vesicular transport protein disorders
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- STX7 (links | edit)
- STX6 (links | edit)
- COPE (gene) (links | edit)
- AP3B1 (links | edit)
- VAMP3 (links | edit)
- STX5 (links | edit)
- COPB2 (links | edit)
- STX2 (links | edit)
- COPG2 (links | edit)
- COPG (links | edit)
- STX12 (links | edit)
- STX8 (links | edit)
- Syntaxin binding protein 2 (links | edit)
- DNM3 (links | edit)
- AP1S2 (links | edit)
- SNAP29 (links | edit)
- SYT2 (links | edit)
- SYT3 (links | edit)
- SYT9 (links | edit)
- VAMP1 (links | edit)
- STX16 (links | edit)
- SYT11 (links | edit)
- VPS33B (links | edit)
- SYT5 (links | edit)
- SYT13 (links | edit)
- SYT4 (links | edit)
- SYT7 (links | edit)
- COPZ1 (links | edit)
- Caveolin 2 (links | edit)
- SYT6 (links | edit)
- STX1B (links | edit)
- X-linked intellectual disability (transclusion) (links | edit)
- Congenital generalized lipodystrophy (transclusion) (links | edit)
- Syntaxin 3 (links | edit)
- Syntaxin (links | edit)
- Sorting nexin (links | edit)
- Arthrogryposis–renal dysfunction–cholestasis syndrome (transclusion) (links | edit)
- CEDNIK syndrome (transclusion) (links | edit)
- Munc-18 (links | edit)
- Cranio-lenticulo-sutural dysplasia (transclusion) (links | edit)
- Inherited disorders of trafficking (transclusion) (links | edit)
- Vacuolar protein sorting (links | edit)
- Active zone (links | edit)
- SEC24A (links | edit)
- Clathrin adaptor protein (links | edit)
- Biogenesis of lysosome-related organelles complex 3 (links | edit)
- Halperin-Birk syndrome (transclusion) (links | edit)
- User:Triplesugariron (links | edit)
- User:NussPoyava/sandbox (transclusion) (links | edit)
- User:NSH002/t (links | edit)