ENST00000220616.9:c.8041T>G
MANE Select
|
ENSP00000220616.4:p.Phe2681Val
|
|
ENST00000220616.8:c.8041T>G
|
ENSP00000220616.4:p.Phe2681Val
|
|
ENST00000519178.5:c.3407T>G
|
|
|
ENST00000519543.5:c.2440T>G
|
ENSP00000430430.1:p.Phe814Val
|
|
ENST00000521107.1:c.253T>G
|
ENSP00000430161.1:p.Phe85Val
|
|
ENST00000522691.1:n.127T>G
|
|
|
ENST00000523756.5:c.4696T>G
|
|
|
NM_003235.4:c.8041T>G
|
NP_003226.4:p.Phe2681Val
|
|
XM_005251038.3:c.7849T>G
|
XP_005251095.1:p.Phe2617Val
|
|
XM_006716622.2:c.7978T>G
|
XP_006716685.1:p.Phe2660Val
|
|
XM_005251038.4:c.7849T>G
|
XP_005251095.1:p.Phe2617Val
|
|
XM_006716622.3:c.7978T>G
|
XP_006716685.1:p.Phe2660Val
|
|
XM_017013793.1:c.7975T>G
|
XP_016869282.1:p.Phe2659Val
|
|
XM_017013794.1:c.7906T>G
|
XP_016869283.1:p.Phe2636Val
|
|
XM_017013795.1:c.7870T>G
|
XP_016869284.1:p.Phe2624Val
|
|
XM_017013796.1:c.7822T>G
|
XP_016869285.1:p.Phe2608Val
|
|
XM_017013797.1:c.7780T>G
|
XP_016869286.1:p.Phe2594Val
|
|
NM_003235.5:c.8041T>G
MANE Select
|
NP_003226.4:p.Phe2681Val
|
|