ENST00000585465.3:c.816C>T
|
ENSP00000490268.2:p.Tyr272=
|
|
ENST00000585748.3:c.444C>T
|
ENSP00000477641.2:p.Tyr148=
|
|
ENST00000585851.2:c.642C>T
|
ENSP00000467912.2:p.Tyr214=
|
|
ENST00000326873.12:c.816C>T
MANE Select
|
ENSP00000324856.6:p.Tyr272=
|
|
ENST00000652231.1:c.816C>T
|
ENSP00000498804.1:p.Tyr272=
|
|
ENST00000326873.11:c.816C>T
|
ENSP00000324856.6:p.Tyr272=
|
|
ENST00000586243.5:c.816C>T
|
ENSP00000467240.2:p.Tyr272=
|
|
ENST00000586358.5:n.714C>T
|
|
|
ENST00000589152.5:n.906C>T
|
|
|
ENST00000591133.2:n.787C>T
|
|
|
NM_000455.4:c.816C>T , LRG_319t1:c.816C>T
|
NP_000446.1:p.Tyr272=
|
|
XM_005259617.1:c.816C>T
|
XP_005259674.1:p.Tyr272=
|
|
XM_005259618.3:c.816C>T
|
XP_005259675.1:p.Tyr272=
|
|
XM_011528209.1:c.594C>T
|
XP_011526511.1:p.Tyr198=
|
|
XR_936204.1:n.1441C>T
|
|
|
XM_005259617.3:c.816C>T
|
XP_005259674.1:p.Tyr272=
|
|
XM_011528209.2:c.594C>T
|
XP_011526511.1:p.Tyr198=
|
|
XR_001753738.2:n.1441C>T
|
|
|
XR_001753739.1:n.1441C>T
|
|
|
XR_001753740.2:n.1441C>T
|
|
|
NM_000455.5:c.816C>T
MANE Select
|
NP_000446.1:p.Tyr272=
|
|