ENST00000269980.7:c.950C>T
MANE Select
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ENSP00000269980.2:p.Ala317Val
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ENST00000269980.6:c.950C>T
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ENSP00000269980.2:p.Ala317Val
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ENST00000457836.6:c.884C>T
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ENSP00000416000.2:p.Ala295Val
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ENST00000535632.5:n.579C>T
|
|
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ENST00000540732.3:c.1052C>T
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ENSP00000443246.1:p.Ala351Val
|
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ENST00000542943.5:c.863C>T
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ENSP00000440345.1:p.Ala288Val
|
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ENST00000545787.1:n.578C>T
|
|
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ENST00000595085.5:c.922+28C>T
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ENSP00000471150.2:n.922+28C>T
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NM_000709.3:c.950C>T
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NP_000700.1:p.Ala317Val
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NM_001164783.1:c.947C>T
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NP_001158255.1:p.Ala316Val
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NM_000709.4:c.950C>T
MANE Select
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NP_000700.1:p.Ala317Val
|
|
NM_001164783.2:c.947C>T
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NP_001158255.1:p.Ala316Val
|
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