ENST00000269980.7:c.663C=
MANE Select
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ENSP00000269980.2:p.Tyr221=
|
|
ENST00000269980.6:c.663C=
|
ENSP00000269980.2:p.Tyr221=
|
|
ENST00000457836.6:c.597C=
|
ENSP00000416000.2:p.Tyr199=
|
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ENST00000535632.5:n.292C=
|
|
|
ENST00000538423.5:n.789C=
|
|
|
ENST00000540732.3:c.765C=
|
ENSP00000443246.1:p.Tyr255=
|
|
ENST00000541315.1:c.563C=
|
|
|
ENST00000542943.5:c.576C=
|
ENSP00000440345.1:p.Tyr192=
|
|
ENST00000545787.1:n.291C=
|
|
|
ENST00000595085.5:c.663C=
|
ENSP00000471150.2:p.Tyr221=
|
|
NM_000709.3:c.663C=
|
NP_000700.1:p.Tyr221=
|
|
NM_001164783.1:c.663C=
|
NP_001158255.1:p.Tyr221=
|
|
NM_000709.4:c.663C=
MANE Select
|
NP_000700.1:p.Tyr221=
|
|
NM_001164783.2:c.663C=
|
NP_001158255.1:p.Tyr221=
|
|