ENST00000205402.10:c.872T>C
MANE Select
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ENSP00000205402.3:p.Val291Ala
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ENST00000205402.9:c.872T>C
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ENSP00000205402.3:p.Val291Ala
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ENST00000415325.5:c.*546T>C
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ENSP00000402593.1:n.*546T>C
|
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ENST00000417551.5:c.872T>C
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ENSP00000390667.1:p.Val291Ala
|
|
ENST00000437604.6:c.728T>C
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ENSP00000387542.2:p.Val243Ala
|
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ENST00000440410.5:c.803T>C
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ENSP00000417016.1:p.Val268Ala
|
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NM_000108.4:c.872T>C
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NP_000099.2:p.Val291Ala
|
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NM_001289750.1:c.575T>C
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NP_001276679.1:p.Val192Ala
|
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NM_001289751.1:c.803T>C
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NP_001276680.1:p.Val268Ala
|
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NM_001289752.1:c.728T>C
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NP_001276681.1:p.Val243Ala
|
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NM_000108.5:c.872T>C
MANE Select
|
NP_000099.2:p.Val291Ala
|
|