ENST00000357578.8:c.1259T>G
MANE Select
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ENSP00000350191.3:p.Phe420Cys
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ENST00000479394.2:n.374T>G
|
|
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ENST00000672352.1:c.878T>G
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ENSP00000500876.1:p.Phe293Cys
|
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ENST00000672652.1:c.1222T>G
|
|
|
ENST00000348925.2:c.1298T>G
|
ENSP00000314649.3:p.Phe433Cys
|
|
ENST00000357578.7:c.1259T>G
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ENSP00000350191.3:p.Phe420Cys
|
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ENST00000479394.1:n.374T>G
|
|
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ENST00000491546.5:c.1175T>G
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ENSP00000417687.1:p.Phe392Cys
|
|
NM_001080.3:c.1259T>G
MANE Select
|
NP_001071.1:p.Phe420Cys
|
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NM_170740.1:c.1298T>G
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NP_733936.1:p.Phe433Cys
|
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NM_001368954.1:c.1115T>G
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NP_001355883.1:p.Phe372Cys
|
|