ENST00000215882.10:c.587C>T
MANE Select
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ENSP00000215882.5:p.Ala196Val
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ENST00000215882.9:c.587C>T
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ENSP00000215882.5:p.Ala196Val
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ENST00000451283.5:c.278C>T
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ENSP00000401480.1:p.Ala93Val
|
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ENST00000461267.1:n.733C>T
|
|
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ENST00000470922.5:n.729C>T
|
|
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NM_001256534.1:c.608C>T
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NP_001243463.1:p.Ala203Val
|
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NM_001287387.1:c.278C>T
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NP_001274316.1:p.Ala93Val
|
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NM_005984.4:c.587C>T
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NP_005975.1:p.Ala196Val
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NR_046298.2:n.638C>T
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|
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NM_005984.5:c.587C>T
MANE Select
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NP_005975.1:p.Ala196Val
|
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NM_001256534.2:c.608C>T
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NP_001243463.1:p.Ala203Val
|
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NM_001287387.2:c.278C>T
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NP_001274316.1:p.Ala93Val
|
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NR_046298.3:n.511C>T
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