ENST00000269980.7:c.771G>A
MANE Select
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ENSP00000269980.2:p.Glu257=
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ENST00000269980.6:c.771G>A
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ENSP00000269980.2:p.Glu257=
|
|
ENST00000457836.6:c.705G>A
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ENSP00000416000.2:p.Glu235=
|
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ENST00000535632.5:n.400G>A
|
|
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ENST00000540732.3:c.873G>A
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ENSP00000443246.1:p.Glu291=
|
|
ENST00000542943.5:c.684G>A
|
ENSP00000440345.1:p.Glu228=
|
|
ENST00000545787.1:n.399G>A
|
|
|
ENST00000595085.5:c.771G>A
|
ENSP00000471150.2:p.Glu257=
|
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NM_000709.3:c.771G>A
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NP_000700.1:p.Glu257=
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NM_001164783.1:c.771G>A
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NP_001158255.1:p.Glu257=
|
|
NM_000709.4:c.771G>A
MANE Select
|
NP_000700.1:p.Glu257=
|
|
NM_001164783.2:c.771G>A
|
NP_001158255.1:p.Glu257=
|
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