ENST00000209873.9:c.1531T>A
MANE Select
|
ENSP00000209873.4:p.Ser511Thr
|
|
ENST00000546562.6:n.2595T>A
|
|
|
ENST00000547238.6:n.2167T>A
|
|
|
ENST00000547520.6:n.1647T>A
|
|
|
ENST00000547757.2:c.*449T>A
|
ENSP00000448020.2:n.*449T>A
|
|
ENST00000548931.6:c.966T>A
|
ENSP00000457518.1:p.Ala322=
|
|
ENST00000549450.6:n.1465T>A
|
|
|
ENST00000672797.1:n.2020T>A
|
|
|
ENST00000209873.8:c.1531T>A
|
ENSP00000209873.4:p.Ser511Thr
|
|
ENST00000394384.7:c.1432T>A
|
ENSP00000377908.3:p.Ser478Thr
|
|
ENST00000548931.5:c.966T>A
|
ENSP00000457518.1:p.Ala322=
|
|
ENST00000550286.5:c.1159T>A
|
ENSP00000446885.1:p.Ser387Thr
|
|
ENST00000552876.5:n.1874T>A
|
|
|
NM_001173466.1:c.1432T>A
|
NP_001166937.1:p.Ser478Thr
|
|
NM_015665.5:c.1531T>A
|
NP_056480.1:p.Ser511Thr
|
|
XM_006719617.2:c.1546T>A
|
XP_006719680.1:p.Ser516Thr
|
|
XM_011538777.1:c.1588T>A
|
XP_011537079.1:p.Ser530Thr
|
|
XM_011538778.1:c.1573T>A
|
XP_011537080.1:p.Ser525Thr
|
|
XM_011538779.1:c.1489T>A
|
XP_011537081.1:p.Ser497Thr
|
|
XM_011538780.1:c.1474T>A
|
XP_011537082.1:p.Ser492Thr
|
|
XM_011538781.1:c.922T>A
|
XP_011537083.1:p.Ser308Thr
|
|
XM_011538778.2:c.1573T>A
|
XP_011537080.1:p.Ser525Thr
|
|
XM_011538780.2:c.1474T>A
|
XP_011537082.1:p.Ser492Thr
|
|
XR_001748875.2:n.1588T>A
|
|
|
NM_015665.6:c.1531T>A
MANE Select
|
NP_056480.1:p.Ser511Thr
|
|
NM_001173466.2:c.1432T>A
|
NP_001166937.1:p.Ser478Thr
|
|