ENST00000209873.9:c.922T>A
MANE Select
|
ENSP00000209873.4:p.Ser308Thr
|
|
ENST00000546393.7:n.1767T>A
|
|
|
ENST00000546562.6:n.1986T>A
|
|
|
ENST00000547238.6:n.1558T>A
|
|
|
ENST00000547520.6:n.916T>A
|
|
|
ENST00000547757.2:c.-30T>A
|
ENSP00000448020.2:n.-30T>A
|
|
ENST00000548880.2:n.1372T>A
|
|
|
ENST00000548931.6:c.442T>A
|
ENSP00000457518.1:p.Ser148Thr
|
|
ENST00000549450.6:n.856T>A
|
|
|
ENST00000552161.6:n.1878T>A
|
|
|
ENST00000672797.1:n.1375T>A
|
|
|
ENST00000672900.1:n.1720T>A
|
|
|
ENST00000209873.8:c.922T>A
|
ENSP00000209873.4:p.Ser308Thr
|
|
ENST00000394384.7:c.823T>A
|
ENSP00000377908.3:p.Ser275Thr
|
|
ENST00000546393.6:n.819T>A
|
|
|
ENST00000546572.1:n.374T>A
|
|
|
ENST00000547520.5:n.626T>A
|
|
|
ENST00000547757.1:c.823T>A
|
ENSP00000448020.1:p.Ser275Thr
|
|
ENST00000547761.6:n.814T>A
|
|
|
ENST00000548931.5:c.442T>A
|
ENSP00000457518.1:p.Ser148Thr
|
|
ENST00000550033.5:n.177T>A
|
|
|
ENST00000550286.5:c.550T>A
|
ENSP00000446885.1:p.Ser184Thr
|
|
ENST00000552876.5:n.1265T>A
|
|
|
NM_001173466.1:c.823T>A
|
NP_001166937.1:p.Ser275Thr
|
|
NM_015665.5:c.922T>A
|
NP_056480.1:p.Ser308Thr
|
|
XM_006719617.2:c.937T>A
|
XP_006719680.1:p.Ser313Thr
|
|
XM_006719619.2:c.937T>A
|
XP_006719682.1:p.Ser313Thr
|
|
XM_011538777.1:c.937T>A
|
XP_011537079.1:p.Ser313Thr
|
|
XM_011538778.1:c.922T>A
|
XP_011537080.1:p.Ser308Thr
|
|
XM_011538779.1:c.838T>A
|
XP_011537081.1:p.Ser280Thr
|
|
XM_011538780.1:c.823T>A
|
XP_011537082.1:p.Ser275Thr
|
|
XM_011538781.1:c.271T>A
|
XP_011537083.1:p.Ser91Thr
|
|
XM_011538778.2:c.922T>A
|
XP_011537080.1:p.Ser308Thr
|
|
XM_011538780.2:c.823T>A
|
XP_011537082.1:p.Ser275Thr
|
|
XR_001748875.2:n.943T>A
|
|
|
NM_015665.6:c.922T>A
MANE Select
|
NP_056480.1:p.Ser308Thr
|
|
NM_001173466.2:c.823T>A
|
NP_001166937.1:p.Ser275Thr
|
|