ENST00000209873.9:c.1056G>T
MANE Select
|
ENSP00000209873.4:p.Leu352=
|
|
ENST00000546562.6:n.2120G>T
|
|
|
ENST00000547238.6:n.1692G>T
|
|
|
ENST00000547520.6:n.1050G>T
|
|
|
ENST00000547757.2:c.105G>T
|
ENSP00000448020.2:p.Leu35=
|
|
ENST00000548880.2:n.1506G>T
|
|
|
ENST00000548931.6:c.576G>T
|
ENSP00000457518.1:p.Leu192=
|
|
ENST00000549450.6:n.990G>T
|
|
|
ENST00000552161.6:n.2012G>T
|
|
|
ENST00000672797.1:n.1545G>T
|
|
|
ENST00000672900.1:n.1998G>T
|
|
|
ENST00000209873.8:c.1056G>T
|
ENSP00000209873.4:p.Leu352=
|
|
ENST00000394384.7:c.957G>T
|
ENSP00000377908.3:p.Leu319=
|
|
ENST00000547520.5:n.760G>T
|
|
|
ENST00000548931.5:c.576G>T
|
ENSP00000457518.1:p.Leu192=
|
|
ENST00000550033.5:n.311G>T
|
|
|
ENST00000550286.5:c.684G>T
|
ENSP00000446885.1:p.Leu228=
|
|
ENST00000552876.5:n.1399G>T
|
|
|
NM_001173466.1:c.957G>T
|
NP_001166937.1:p.Leu319=
|
|
NM_015665.5:c.1056G>T
|
NP_056480.1:p.Leu352=
|
|
XM_006719617.2:c.1071G>T
|
XP_006719680.1:p.Leu357=
|
|
XM_011538777.1:c.1071G>T
|
XP_011537079.1:p.Leu357=
|
|
XM_011538778.1:c.1056G>T
|
XP_011537080.1:p.Leu352=
|
|
XM_011538779.1:c.972G>T
|
XP_011537081.1:p.Leu324=
|
|
XM_011538780.1:c.957G>T
|
XP_011537082.1:p.Leu319=
|
|
XM_011538781.1:c.405G>T
|
XP_011537083.1:p.Leu135=
|
|
XM_011538778.2:c.1056G>T
|
XP_011537080.1:p.Leu352=
|
|
XM_011538780.2:c.957G>T
|
XP_011537082.1:p.Leu319=
|
|
XR_001748875.2:n.1113G>T
|
|
|
NM_015665.6:c.1056G>T
MANE Select
|
NP_056480.1:p.Leu352=
|
|
NM_001173466.2:c.957G>T
|
NP_001166937.1:p.Leu319=
|
|