|
NM_006767.4:c.2244C>G
MANE Select
|
NP_006758.2:p.Tyr748Ter
|
|
ENST00000646124.2:c.2244C>G
MANE Select
|
ENSP00000496779.1:p.Tyr748Ter
|
|
NM_006767.3:c.2244C>G
|
NP_006758.2:p.Tyr748Ter
|
|
ENST00000215739.12:c.2244C>G
|
ENSP00000215739.8:p.Tyr748Ter
|
|
ENST00000415817.1:c.142C>G
|
|
|
ENST00000415817.2:c.673C>G
|
|
|
ENST00000452988.5:c.406C>G
|
ENSP00000408789.1:n.406C>G
|
|
ENST00000463909.1:n.1542C>G
|
|
|
ENST00000479606.5:n.2390C>G
|
|
|
ENST00000495142.6:n.2596C>G
|
|
|
ENST00000498649.1:n.260C>G
|
|
|
ENST00000642151.1:c.2075C>G
|
|
|
ENST00000643578.1:n.2266C>G
|
|
|
ENST00000643710.1:n.1105C>G
|
|
|
ENST00000646506.1:n.2111C>G
|
|
|
ENST00000700578.1:c.2244C>G
|
ENSP00000515073.1:p.Tyr748Ter
|