ENST00000695651.1:n.902T>G
|
|
|
ENST00000695652.1:c.2431T>G
|
ENSP00000512083.1:p.Tyr811Asp
|
|
ENST00000695653.1:c.463T>G
|
ENSP00000512084.1:p.Tyr155Asp
|
|
ENST00000695654.1:c.1678T>G
|
ENSP00000512085.1:p.Tyr560Asp
|
|
ENST00000695655.1:c.1495T>G
|
ENSP00000512086.1:n.1495T>G
|
|
ENST00000695692.1:n.1918T>G
|
|
|
ENST00000245907.11:c.2554T>G
MANE Select
|
ENSP00000245907.4:p.Tyr852Asp
|
|
ENST00000245907.10:c.2554T>G
|
ENSP00000245907.4:p.Tyr852Asp
|
|
ENST00000594005.1:n.35T>G
|
|
|
ENST00000602053.1:n.602T>G
|
|
|
NM_000064.3:c.2554T>G
|
NP_000055.2:p.Tyr852Asp
|
|
NM_000064.4:c.2554T>G
MANE Select
|
NP_000055.2:p.Tyr852Asp
|
|