ENST00000209873.9:c.1439C>T
MANE Select
|
ENSP00000209873.4:p.Ala480Val
|
|
ENST00000546562.6:n.2503C>T
|
|
|
ENST00000547238.6:n.2075C>T
|
|
|
ENST00000547520.6:n.1555C>T
|
|
|
ENST00000547757.2:c.*357C>T
|
ENSP00000448020.2:n.*357C>T
|
|
ENST00000548880.2:n.1889C>T
|
|
|
ENST00000548931.6:c.874C>T
|
ENSP00000457518.1:p.Pro292Ser
|
|
ENST00000549450.6:n.1373C>T
|
|
|
ENST00000552161.6:n.2517C>T
|
|
|
ENST00000672797.1:n.1928C>T
|
|
|
ENST00000209873.8:c.1439C>T
|
ENSP00000209873.4:p.Ala480Val
|
|
ENST00000394384.7:c.1340C>T
|
ENSP00000377908.3:p.Ala447Val
|
|
ENST00000548931.5:c.874C>T
|
ENSP00000457518.1:p.Pro292Ser
|
|
ENST00000550286.5:c.1067C>T
|
ENSP00000446885.1:p.Ala356Val
|
|
ENST00000552876.5:n.1782C>T
|
|
|
NM_001173466.1:c.1340C>T
|
NP_001166937.1:p.Ala447Val
|
|
NM_015665.5:c.1439C>T
|
NP_056480.1:p.Ala480Val
|
|
XM_006719617.2:c.1454C>T
|
XP_006719680.1:p.Ala485Val
|
|
XM_011538777.1:c.1496C>T
|
XP_011537079.1:p.Ala499Val
|
|
XM_011538778.1:c.1481C>T
|
XP_011537080.1:p.Ala494Val
|
|
XM_011538779.1:c.1397C>T
|
XP_011537081.1:p.Ala466Val
|
|
XM_011538780.1:c.1382C>T
|
XP_011537082.1:p.Ala461Val
|
|
XM_011538781.1:c.830C>T
|
XP_011537083.1:p.Ala277Val
|
|
XM_011538778.2:c.1481C>T
|
XP_011537080.1:p.Ala494Val
|
|
XM_011538780.2:c.1382C>T
|
XP_011537082.1:p.Ala461Val
|
|
XR_001748875.2:n.1496C>T
|
|
|
NM_015665.6:c.1439C>T
MANE Select
|
NP_056480.1:p.Ala480Val
|
|
NM_001173466.2:c.1340C>T
|
NP_001166937.1:p.Ala447Val
|
|