ENST00000695651.1:n.1040T>G
|
|
|
ENST00000695652.1:c.2569T>G
|
ENSP00000512083.1:p.Tyr857Asp
|
|
ENST00000695653.1:c.601T>G
|
ENSP00000512084.1:p.Tyr201Asp
|
|
ENST00000695654.1:c.1816T>G
|
ENSP00000512085.1:p.Tyr606Asp
|
|
ENST00000695655.1:c.1633T>G
|
ENSP00000512086.1:n.1633T>G
|
|
ENST00000695692.1:n.2056T>G
|
|
|
ENST00000245907.11:c.2692T>G
MANE Select
|
ENSP00000245907.4:p.Tyr898Asp
|
|
ENST00000245907.10:c.2692T>G
|
ENSP00000245907.4:p.Tyr898Asp
|
|
ENST00000594005.1:n.268T>G
|
|
|
NM_000064.3:c.2692T>G
|
NP_000055.2:p.Tyr898Asp
|
|
NM_000064.4:c.2692T>G
MANE Select
|
NP_000055.2:p.Tyr898Asp
|
|