ENST00000695651.1:n.1042T>G
|
|
|
ENST00000695652.1:c.2571T>G
|
ENSP00000512083.1:p.Tyr857Ter
|
|
ENST00000695653.1:c.603T>G
|
ENSP00000512084.1:p.Tyr201Ter
|
|
ENST00000695654.1:c.1818T>G
|
ENSP00000512085.1:p.Tyr606Ter
|
|
ENST00000695655.1:c.1635T>G
|
ENSP00000512086.1:n.1635T>G
|
|
ENST00000695692.1:n.2058T>G
|
|
|
ENST00000245907.11:c.2694T>G
MANE Select
|
ENSP00000245907.4:p.Tyr898Ter
|
|
ENST00000245907.10:c.2694T>G
|
ENSP00000245907.4:p.Tyr898Ter
|
|
ENST00000594005.1:n.270T>G
|
|
|
NM_000064.3:c.2694T>G
|
NP_000055.2:p.Tyr898Ter
|
|
NM_000064.4:c.2694T>G
MANE Select
|
NP_000055.2:p.Tyr898Ter
|
|