ENST00000366669.9:c.1896G>T
MANE Select
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ENSP00000355629.4:p.Gln632His
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ENST00000366668.7:c.1893G>T
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ENSP00000355628.3:p.Gln631His
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ENST00000366669.8:c.1896G>T
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ENSP00000355629.4:p.Gln632His
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ENST00000468893.6:c.*1754G>T
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ENSP00000476305.1:n.*1754G>T
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ENST00000478710.1:n.155G>T
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ENST00000490900.1:n.675G>T
|
|
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ENST00000534989.1:c.1719G>T
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ENSP00000440349.1:p.Gln573His
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NM_001145036.1:c.1893G>T
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NP_001138508.1:p.Gln631His
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NM_007357.2:c.1896G>T
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NP_031383.1:p.Gln632His
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NM_007357.3:c.1896G>T
MANE Select
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NP_031383.1:p.Gln632His
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NM_001145036.2:c.1893G>T
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NP_001138508.1:p.Gln631His
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