ENST00000205402.10:c.1182C>T
MANE Select
|
ENSP00000205402.3:p.Tyr394=
|
|
ENST00000205402.9:c.1182C>T
|
ENSP00000205402.3:p.Tyr394=
|
|
ENST00000415325.5:c.*856C>T
|
ENSP00000402593.1:n.*856C>T
|
|
ENST00000417551.5:c.1182C>T
|
ENSP00000390667.1:p.Tyr394=
|
|
ENST00000437604.6:c.1038C>T
|
ENSP00000387542.2:p.Tyr346=
|
|
ENST00000440410.5:c.1113C>T
|
ENSP00000417016.1:p.Tyr371=
|
|
NM_000108.4:c.1182C>T
|
NP_000099.2:p.Tyr394=
|
|
NM_001289750.1:c.885C>T
|
NP_001276679.1:p.Tyr295=
|
|
NM_001289751.1:c.1113C>T
|
NP_001276680.1:p.Tyr371=
|
|
NM_001289752.1:c.1038C>T
|
NP_001276681.1:p.Tyr346=
|
|
NM_000108.5:c.1182C>T
MANE Select
|
NP_000099.2:p.Tyr394=
|
|