ENST00000209873.9:c.1630T>G
MANE Select
|
ENSP00000209873.4:p.Ser544Ala
|
|
ENST00000547757.2:c.*548T>G
|
ENSP00000448020.2:n.*548T>G
|
|
ENST00000548931.6:c.1065T>G
|
ENSP00000457518.1:p.Ile355Met
|
|
ENST00000549450.6:n.1564T>G
|
|
|
ENST00000209873.8:c.1630T>G
|
ENSP00000209873.4:p.Ser544Ala
|
|
ENST00000394384.7:c.1531T>G
|
ENSP00000377908.3:p.Ser511Ala
|
|
ENST00000548931.5:c.1065T>G
|
ENSP00000457518.1:p.Ile355Met
|
|
ENST00000550286.5:c.1258T>G
|
ENSP00000446885.1:p.Ser420Ala
|
|
ENST00000552876.5:n.1973T>G
|
|
|
NM_001173466.1:c.1531T>G
|
NP_001166937.1:p.Ser511Ala
|
|
NM_015665.5:c.1630T>G
|
NP_056480.1:p.Ser544Ala
|
|
XM_006719617.2:c.1645T>G
|
XP_006719680.1:p.Ser549Ala
|
|
XM_011538777.1:c.1687T>G
|
XP_011537079.1:p.Ser563Ala
|
|
XM_011538778.1:c.1672T>G
|
XP_011537080.1:p.Ser558Ala
|
|
XM_011538779.1:c.1588T>G
|
XP_011537081.1:p.Ser530Ala
|
|
XM_011538780.1:c.1573T>G
|
XP_011537082.1:p.Ser525Ala
|
|
XM_011538781.1:c.1021T>G
|
XP_011537083.1:p.Ser341Ala
|
|
XM_011538778.2:c.1672T>G
|
XP_011537080.1:p.Ser558Ala
|
|
XM_011538780.2:c.1573T>G
|
XP_011537082.1:p.Ser525Ala
|
|
XR_001748875.2:n.1687T>G
|
|
|
NM_015665.6:c.1630T>G
MANE Select
|
NP_056480.1:p.Ser544Ala
|
|
NM_001173466.2:c.1531T>G
|
NP_001166937.1:p.Ser511Ala
|
|