ENST00000614565.5:c.1806G>T
MANE Select
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ENSP00000484928.1:p.Gln602His
|
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ENST00000543233.2:c.1584G>T
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ENSP00000443301.1:p.Gln528His
|
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ENST00000611855.4:c.1524G>T
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ENSP00000480844.1:p.Gln508His
|
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ENST00000614565.4:c.1806G>T
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ENSP00000484928.1:p.Gln602His
|
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NM_001252338.2:c.1695G>T
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NP_001239267.1:p.Gln565His
|
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NM_001252339.2:c.1584G>T
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NP_001239268.1:p.Gln528His
|
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NM_001794.4:c.1806G>T
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NP_001785.2:p.Gln602His
|
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NM_001794.5:c.1806G>T
MANE Select
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NP_001785.2:p.Gln602His
|
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NM_001252339.3:c.1584G>T
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NP_001239268.1:p.Gln528His
|
|