ENST00000269980.7:c.872A=
MANE Select
|
ENSP00000269980.2:p.Tyr291=
|
|
ENST00000269980.6:c.872A=
|
ENSP00000269980.2:p.Tyr291=
|
|
ENST00000457836.6:c.806A=
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ENSP00000416000.2:p.Tyr269=
|
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ENST00000535632.5:n.501A=
|
|
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ENST00000540732.3:c.974A=
|
ENSP00000443246.1:p.Tyr325=
|
|
ENST00000542943.5:c.785A=
|
ENSP00000440345.1:p.Tyr262=
|
|
ENST00000545787.1:n.500A=
|
|
|
ENST00000595085.5:c.872A=
|
ENSP00000471150.2:p.Tyr291=
|
|
NM_000709.3:c.872A=
|
NP_000700.1:p.Tyr291=
|
|
NM_001164783.1:c.869A=
|
NP_001158255.1:p.Tyr290=
|
|
NM_000709.4:c.872A=
MANE Select
|
NP_000700.1:p.Tyr291=
|
|
NM_001164783.2:c.869A=
|
NP_001158255.1:p.Tyr290=
|
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