ENST00000262461.7:c.3615G>T
MANE Select
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ENSP00000262461.2:p.Gln1205His
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ENST00000262461.6:c.3615G>T
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ENSP00000262461.2:p.Gln1205His
|
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ENST00000343225.4:c.3567G>T
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ENSP00000340878.4:p.Gln1189His
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ENST00000509205.5:c.*228G>T
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ENSP00000427109.1:n.*228G>T
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NM_001046.2:c.3615G>T
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NP_001037.1:p.Gln1205His
|
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NM_001256461.1:c.3567G>T
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NP_001243390.1:p.Gln1189His
|
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NR_046207.1:n.3845G>T
|
|
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XM_017009771.1:c.1857G>T
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XP_016865260.1:p.Gln619His
|
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XR_001742214.1:n.3839G>T
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|
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NM_001046.3:c.3615G>T
MANE Select
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NP_001037.1:p.Gln1205His
|
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NM_001256461.2:c.3567G>T
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NP_001243390.1:p.Gln1189His
|
|
NR_046207.2:n.3870G>T
|
|
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