ENST00000209873.9:c.1552T>A
MANE Select
|
ENSP00000209873.4:p.Phe518Ile
|
|
ENST00000546562.6:n.2616T>A
|
|
|
ENST00000547238.6:n.2188T>A
|
|
|
ENST00000547520.6:n.1668T>A
|
|
|
ENST00000547757.2:c.*470T>A
|
ENSP00000448020.2:n.*470T>A
|
|
ENST00000548931.6:c.987T>A
|
ENSP00000457518.1:p.Ser329=
|
|
ENST00000549450.6:n.1486T>A
|
|
|
ENST00000672797.1:n.2041T>A
|
|
|
ENST00000209873.8:c.1552T>A
|
ENSP00000209873.4:p.Phe518Ile
|
|
ENST00000394384.7:c.1453T>A
|
ENSP00000377908.3:p.Phe485Ile
|
|
ENST00000548931.5:c.987T>A
|
ENSP00000457518.1:p.Ser329=
|
|
ENST00000550286.5:c.1180T>A
|
ENSP00000446885.1:p.Phe394Ile
|
|
ENST00000552876.5:n.1895T>A
|
|
|
NM_001173466.1:c.1453T>A
|
NP_001166937.1:p.Phe485Ile
|
|
NM_015665.5:c.1552T>A
|
NP_056480.1:p.Phe518Ile
|
|
XM_006719617.2:c.1567T>A
|
XP_006719680.1:p.Phe523Ile
|
|
XM_011538777.1:c.1609T>A
|
XP_011537079.1:p.Phe537Ile
|
|
XM_011538778.1:c.1594T>A
|
XP_011537080.1:p.Phe532Ile
|
|
XM_011538779.1:c.1510T>A
|
XP_011537081.1:p.Phe504Ile
|
|
XM_011538780.1:c.1495T>A
|
XP_011537082.1:p.Phe499Ile
|
|
XM_011538781.1:c.943T>A
|
XP_011537083.1:p.Phe315Ile
|
|
XM_011538778.2:c.1594T>A
|
XP_011537080.1:p.Phe532Ile
|
|
XM_011538780.2:c.1495T>A
|
XP_011537082.1:p.Phe499Ile
|
|
XR_001748875.2:n.1609T>A
|
|
|
NM_015665.6:c.1552T>A
MANE Select
|
NP_056480.1:p.Phe518Ile
|
|
NM_001173466.2:c.1453T>A
|
NP_001166937.1:p.Phe485Ile
|
|