ENST00000695651.1:n.857T>A
|
|
|
ENST00000695652.1:c.2386T>A
|
ENSP00000512083.1:p.Tyr796Asn
|
|
ENST00000695653.1:c.418T>A
|
ENSP00000512084.1:p.Tyr140Asn
|
|
ENST00000695654.1:c.1633T>A
|
ENSP00000512085.1:p.Tyr545Asn
|
|
ENST00000695655.1:c.1450T>A
|
ENSP00000512086.1:n.1450T>A
|
|
ENST00000695692.1:n.1873T>A
|
|
|
ENST00000245907.11:c.2509T>A
MANE Select
|
ENSP00000245907.4:p.Tyr837Asn
|
|
ENST00000245907.10:c.2509T>A
|
ENSP00000245907.4:p.Tyr837Asn
|
|
ENST00000602053.1:n.557T>A
|
|
|
NM_000064.3:c.2509T>A
|
NP_000055.2:p.Tyr837Asn
|
|
NM_000064.4:c.2509T>A
MANE Select
|
NP_000055.2:p.Tyr837Asn
|
|