ENST00000269980.7:c.683C>T
MANE Select
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ENSP00000269980.2:p.Ala228Val
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ENST00000269980.6:c.683C>T
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ENSP00000269980.2:p.Ala228Val
|
|
ENST00000457836.6:c.617C>T
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ENSP00000416000.2:p.Ala206Val
|
|
ENST00000535632.5:n.312C>T
|
|
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ENST00000538423.5:n.809C>T
|
|
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ENST00000540732.3:c.785C>T
|
ENSP00000443246.1:p.Ala262Val
|
|
ENST00000541315.1:c.583C>T
|
|
|
ENST00000542943.5:c.596C>T
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ENSP00000440345.1:p.Ala199Val
|
|
ENST00000545787.1:n.311C>T
|
|
|
ENST00000595085.5:c.683C>T
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ENSP00000471150.2:p.Ala228Val
|
|
NM_000709.3:c.683C>T
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NP_000700.1:p.Ala228Val
|
|
NM_001164783.1:c.683C>T
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NP_001158255.1:p.Ala228Val
|
|
NM_000709.4:c.683C>T
MANE Select
|
NP_000700.1:p.Ala228Val
|
|
NM_001164783.2:c.683C>T
|
NP_001158255.1:p.Ala228Val
|
|