ENST00000356392.9:c.1139C=
MANE Select
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ENSP00000348757.3:p.Ala380=
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ENST00000356392.8:c.1139C=
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ENSP00000348757.3:p.Ala380=
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ENST00000586836.5:c.566C=
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ENSP00000467429.1:p.Ala189=
|
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ENST00000591179.5:c.959C=
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ENSP00000466800.1:p.Ala320=
|
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ENST00000591345.5:c.*1058C=
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ENSP00000467313.1:n.*1058C=
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NM_001302453.1:c.977C=
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NP_001289382.1:p.Ala326=
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NM_001302454.1:c.959C=
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NP_001289383.1:p.Ala320=
|
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NM_145045.4:c.1139C=
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NP_659482.3:p.Ala380=
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XM_017026241.1:c.*33C=
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XP_016881730.1:n.*33C=
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NM_145045.5:c.1139C=
MANE Select
|
NP_659482.3:p.Ala380=
|
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NM_001302454.2:c.959C=
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NP_001289383.1:p.Ala320=
|
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