ENST00000265641.10:c.882T>C
MANE Select
|
ENSP00000265641.4:p.Ile294=
|
|
ENST00000265641.9:c.882T>C
|
ENSP00000265641.4:p.Ile294=
|
|
ENST00000376618.6:c.882T>C
|
ENSP00000365803.2:p.Ile294=
|
|
ENST00000538994.1:c.138T>C
|
ENSP00000454332.1:p.Ile46=
|
|
ENST00000539743.5:c.882T>C
|
ENSP00000446108.1:p.Ile294=
|
|
ENST00000540367.5:c.882T>C
|
ENSP00000439084.1:p.Ile294=
|
|
NM_001031847.2:c.882T>C
|
NP_001027017.1:p.Ile294=
|
|
NM_001876.3:c.882T>C
|
NP_001867.2:p.Ile294=
|
|
XM_005273762.1:c.978T>C
|
XP_005273819.1:p.Ile326=
|
|
XM_005273763.1:c.978T>C
|
XP_005273820.1:p.Ile326=
|
|
XM_005273762.3:c.978T>C
|
XP_005273819.1:p.Ile326=
|
|
XM_017017220.1:c.882T>C
|
XP_016872709.1:p.Ile294=
|
|
NM_001876.4:c.882T>C
MANE Select
|
NP_001867.2:p.Ile294=
|
|
NM_001031847.3:c.882T>C
|
NP_001027017.1:p.Ile294=
|
|