ENST00000695651.1:n.904C>G
|
|
|
ENST00000695652.1:c.2433C>G
|
ENSP00000512083.1:p.Tyr811Ter
|
|
ENST00000695653.1:c.465C>G
|
ENSP00000512084.1:p.Tyr155Ter
|
|
ENST00000695654.1:c.1680C>G
|
ENSP00000512085.1:p.Tyr560Ter
|
|
ENST00000695655.1:c.1497C>G
|
ENSP00000512086.1:n.1497C>G
|
|
ENST00000695692.1:n.1920C>G
|
|
|
ENST00000245907.11:c.2556C>G
MANE Select
|
ENSP00000245907.4:p.Tyr852Ter
|
|
ENST00000245907.10:c.2556C>G
|
ENSP00000245907.4:p.Tyr852Ter
|
|
ENST00000594005.1:n.37C>G
|
|
|
ENST00000602053.1:n.604C>G
|
|
|
NM_000064.3:c.2556C>G
|
NP_000055.2:p.Tyr852Ter
|
|
NM_000064.4:c.2556C>G
MANE Select
|
NP_000055.2:p.Tyr852Ter
|
|