ENST00000209873.9:c.1068G>A
MANE Select
|
ENSP00000209873.4:p.Leu356=
|
|
ENST00000546562.6:n.2132G>A
|
|
|
ENST00000547238.6:n.1704G>A
|
|
|
ENST00000547520.6:n.1062G>A
|
|
|
ENST00000547757.2:c.117G>A
|
ENSP00000448020.2:p.Leu39=
|
|
ENST00000548880.2:n.1518G>A
|
|
|
ENST00000548931.6:c.588G>A
|
ENSP00000457518.1:p.Leu196=
|
|
ENST00000549450.6:n.1002G>A
|
|
|
ENST00000552161.6:n.2024G>A
|
|
|
ENST00000672797.1:n.1557G>A
|
|
|
ENST00000672900.1:n.2010G>A
|
|
|
ENST00000209873.8:c.1068G>A
|
ENSP00000209873.4:p.Leu356=
|
|
ENST00000394384.7:c.969G>A
|
ENSP00000377908.3:p.Leu323=
|
|
ENST00000548931.5:c.588G>A
|
ENSP00000457518.1:p.Leu196=
|
|
ENST00000550033.5:n.323G>A
|
|
|
ENST00000550286.5:c.696G>A
|
ENSP00000446885.1:p.Leu232=
|
|
ENST00000552876.5:n.1411G>A
|
|
|
NM_001173466.1:c.969G>A
|
NP_001166937.1:p.Leu323=
|
|
NM_015665.5:c.1068G>A
|
NP_056480.1:p.Leu356=
|
|
XM_006719617.2:c.1083G>A
|
XP_006719680.1:p.Leu361=
|
|
XM_011538777.1:c.1083G>A
|
XP_011537079.1:p.Leu361=
|
|
XM_011538778.1:c.1068G>A
|
XP_011537080.1:p.Leu356=
|
|
XM_011538779.1:c.984G>A
|
XP_011537081.1:p.Leu328=
|
|
XM_011538780.1:c.969G>A
|
XP_011537082.1:p.Leu323=
|
|
XM_011538781.1:c.417G>A
|
XP_011537083.1:p.Leu139=
|
|
XM_011538778.2:c.1068G>A
|
XP_011537080.1:p.Leu356=
|
|
XM_011538780.2:c.969G>A
|
XP_011537082.1:p.Leu323=
|
|
XR_001748875.2:n.1125G>A
|
|
|
NM_015665.6:c.1068G>A
MANE Select
|
NP_056480.1:p.Leu356=
|
|
NM_001173466.2:c.969G>A
|
NP_001166937.1:p.Leu323=
|
|