ENST00000269980.7:c.661T=
MANE Select
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ENSP00000269980.2:p.Tyr221=
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ENST00000269980.6:c.661T=
|
ENSP00000269980.2:p.Tyr221=
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|
ENST00000457836.6:c.595T=
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ENSP00000416000.2:p.Tyr199=
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ENST00000535632.5:n.290T=
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|
|
ENST00000538423.5:n.787T=
|
|
|
ENST00000540732.3:c.763T=
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ENSP00000443246.1:p.Tyr255=
|
|
ENST00000541315.1:c.561T=
|
|
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ENST00000542943.5:c.574T=
|
ENSP00000440345.1:p.Tyr192=
|
|
ENST00000545787.1:n.289T=
|
|
|
ENST00000595085.5:c.661T=
|
ENSP00000471150.2:p.Tyr221=
|
|
NM_000709.3:c.661T=
|
NP_000700.1:p.Tyr221=
|
|
NM_001164783.1:c.661T=
|
NP_001158255.1:p.Tyr221=
|
|
NM_000709.4:c.661T=
MANE Select
|
NP_000700.1:p.Tyr221=
|
|
NM_001164783.2:c.661T=
|
NP_001158255.1:p.Tyr221=
|
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