|
NM_006767.4:c.1605C>A
MANE Select
|
NP_006758.2:p.Tyr535Ter
|
|
ENST00000646124.2:c.1605C>A
MANE Select
|
ENSP00000496779.1:p.Tyr535Ter
|
|
NM_006767.3:c.1605C>A
|
NP_006758.2:p.Tyr535Ter
|
|
ENST00000215739.12:c.1605C>A
|
ENSP00000215739.8:p.Tyr535Ter
|
|
ENST00000415354.6:c.33C>A
|
ENSP00000393765.2:p.Tyr11Ter
|
|
ENST00000479606.5:n.1751C>A
|
|
|
ENST00000492480.1:n.654C>A
|
|
|
ENST00000495142.6:n.950C>A
|
|
|
ENST00000642151.1:c.1436C>A
|
|
|
ENST00000643578.1:n.1627C>A
|
|
|
ENST00000643710.1:n.466C>A
|
|
|
ENST00000646506.1:n.1184C>A
|
|
|
ENST00000700578.1:c.1605C>A
|
ENSP00000515073.1:p.Tyr535Ter
|