ENST00000252288.8:c.506G>T
MANE Select
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ENSP00000252288.1:p.Cys169Phe
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ENST00000447102.8:c.506G>T
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ENSP00000403536.2:p.Cys169Phe
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ENST00000591788.3:c.189G>T
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|
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ENST00000640164.1:n.339G>T
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|
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ENST00000640762.1:c.437G>T
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ENSP00000492031.1:p.Cys146Phe
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ENST00000252288.6:c.506G>T
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ENSP00000252288.1:p.Cys169Phe
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ENST00000447102.7:c.506G>T
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ENSP00000403536.2:p.Cys169Phe
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ENST00000591788.2:c.191G>T
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ENSP00000466341.2:p.Cys64Phe
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NM_000156.5:c.506G>T
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NP_000147.1:p.Cys169Phe
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NM_138924.2:c.506G>T
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NP_620279.1:p.Cys169Phe
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NM_000156.6:c.506G>T
MANE Select
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NP_000147.1:p.Cys169Phe
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NM_138924.3:c.506G>T
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NP_620279.1:p.Cys169Phe
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