ENST00000347901.9:c.1316T>A
MANE Select
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ENSP00000334002.4:p.Leu439His
|
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ENST00000310778.5:c.1472T>A
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ENSP00000309392.5:p.Leu491His
|
|
ENST00000341193.9:c.1265T>A
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ENSP00000343170.5:p.Leu422His
|
|
ENST00000347901.8:c.1316T>A
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ENSP00000334002.4:p.Leu439His
|
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ENST00000393939.6:c.1241T>A
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ENSP00000377513.2:p.Leu414His
|
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NM_001079870.1:c.1265T>A
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NP_001073339.1:p.Leu422His
|
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NM_001079871.1:c.1241T>A
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NP_001073340.1:p.Leu414His
|
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NM_177977.2:c.1316T>A
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NP_817084.2:p.Leu439His
|
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NM_001367459.1:c.1412T>A
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NP_001354388.1:p.Leu471His
|
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NM_001367460.1:c.1376T>A
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NP_001354389.1:p.Leu459His
|
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NM_001367461.1:c.1241T>A
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NP_001354390.1:p.Leu414His
|
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NM_001367462.1:c.1241T>A
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NP_001354391.1:p.Leu414His
|
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NM_177977.3:c.1316T>A
MANE Select
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NP_817084.2:p.Leu439His
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