ENST00000376649.8:c.654G>T
MANE Select
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ENSP00000365837.3:p.Gln218His
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ENST00000322060.9:c.570G>T
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ENSP00000324726.5:p.Gln190His
|
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ENST00000376649.7:c.654G>T
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ENSP00000365837.3:p.Gln218His
|
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ENST00000443358.6:c.570G>T
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ENSP00000392451.2:p.Gln190His
|
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ENST00000535067.5:c.358-2138G>T
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ENSP00000443969.1:n.358-2138G>T
|
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ENST00000537484.1:c.579G>T
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ENSP00000440179.1:p.Gln193His
|
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ENST00000542167.2:c.495G>T
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ENSP00000438948.1:p.Gln165His
|
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ENST00000543754.1:n.475G>T
|
|
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NM_001002019.2:c.570G>T
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NP_001002019.1:p.Gln190His
|
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NM_001002020.2:c.570G>T
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NP_001002020.1:p.Gln190His
|
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NM_025215.5:c.654G>T
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NP_079491.2:p.Gln218His
|
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XM_011538768.1:c.255G>T
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XP_011537070.1:p.Gln85His
|
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XM_011538768.3:c.255G>T
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XP_011537070.1:p.Gln85His
|
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XR_001748872.1:n.1109G>T
|
|
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NM_001002019.3:c.570G>T
|
NP_001002019.1:p.Gln190His
|
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NM_001002020.3:c.570G>T
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NP_001002020.1:p.Gln190His
|
|
NM_025215.6:c.654G>T
MANE Select
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NP_079491.2:p.Gln218His
|
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