ENST00000269980.7:c.857C>T
MANE Select
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ENSP00000269980.2:p.Ala286Val
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ENST00000269980.6:c.857C>T
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ENSP00000269980.2:p.Ala286Val
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|
ENST00000457836.6:c.791C>T
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ENSP00000416000.2:p.Ala264Val
|
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ENST00000535632.5:n.486C>T
|
|
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ENST00000540732.3:c.959C>T
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ENSP00000443246.1:p.Ala320Val
|
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ENST00000542943.5:c.770C>T
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ENSP00000440345.1:p.Ala257Val
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ENST00000545787.1:n.485C>T
|
|
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ENST00000595085.5:c.857C>T
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ENSP00000471150.2:p.Ala286Val
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NM_000709.3:c.857C>T
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NP_000700.1:p.Ala286Val
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NM_001164783.1:c.854C>T
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NP_001158255.1:p.Ala285Val
|
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NM_000709.4:c.857C>T
MANE Select
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NP_000700.1:p.Ala286Val
|
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NM_001164783.2:c.854C>T
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NP_001158255.1:p.Ala285Val
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