ENST00000209873.9:c.1426A>T
MANE Select
|
ENSP00000209873.4:p.Thr476Ser
|
|
ENST00000546562.6:n.2490A>T
|
|
|
ENST00000547238.6:n.2062A>T
|
|
|
ENST00000547520.6:n.1542A>T
|
|
|
ENST00000547757.2:c.*344A>T
|
ENSP00000448020.2:n.*344A>T
|
|
ENST00000548880.2:n.1876A>T
|
|
|
ENST00000548931.6:c.861A>T
|
ENSP00000457518.1:p.Pro287=
|
|
ENST00000549450.6:n.1360A>T
|
|
|
ENST00000552161.6:n.2504A>T
|
|
|
ENST00000672797.1:n.1915A>T
|
|
|
ENST00000209873.8:c.1426A>T
|
ENSP00000209873.4:p.Thr476Ser
|
|
ENST00000394384.7:c.1327A>T
|
ENSP00000377908.3:p.Thr443Ser
|
|
ENST00000548931.5:c.861A>T
|
ENSP00000457518.1:p.Pro287=
|
|
ENST00000550286.5:c.1054A>T
|
ENSP00000446885.1:p.Thr352Ser
|
|
ENST00000552876.5:n.1769A>T
|
|
|
NM_001173466.1:c.1327A>T
|
NP_001166937.1:p.Thr443Ser
|
|
NM_015665.5:c.1426A>T
|
NP_056480.1:p.Thr476Ser
|
|
XM_006719617.2:c.1441A>T
|
XP_006719680.1:p.Thr481Ser
|
|
XM_011538777.1:c.1483A>T
|
XP_011537079.1:p.Thr495Ser
|
|
XM_011538778.1:c.1468A>T
|
XP_011537080.1:p.Thr490Ser
|
|
XM_011538779.1:c.1384A>T
|
XP_011537081.1:p.Thr462Ser
|
|
XM_011538780.1:c.1369A>T
|
XP_011537082.1:p.Thr457Ser
|
|
XM_011538781.1:c.817A>T
|
XP_011537083.1:p.Thr273Ser
|
|
XM_011538778.2:c.1468A>T
|
XP_011537080.1:p.Thr490Ser
|
|
XM_011538780.2:c.1369A>T
|
XP_011537082.1:p.Thr457Ser
|
|
XR_001748875.2:n.1483A>T
|
|
|
NM_015665.6:c.1426A>T
MANE Select
|
NP_056480.1:p.Thr476Ser
|
|
NM_001173466.2:c.1327A>T
|
NP_001166937.1:p.Thr443Ser
|
|