ENST00000426263.10:c.1208C>G
MANE Select
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ENSP00000416293.2:p.Ala403Gly
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ENST00000674545.1:n.1825C>G
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ENST00000674765.1:c.1030-818C>G
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ENSP00000501811.1:n.1030-818C>G
|
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ENST00000675112.1:n.1509C>G
|
|
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ENST00000676254.1:n.1657C>G
|
|
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ENST00000426263.7:c.1208C>G
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ENSP00000416293.2:p.Ala403Gly
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ENST00000475162.3:c.416-697C>G
|
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ENST00000630287.2:c.*523C>G
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ENSP00000486694.1:n.*523C>G
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NM_006516.2:c.1208C>G
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NP_006507.2:p.Ala403Gly
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NM_006516.3:c.1208C>G
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NP_006507.2:p.Ala403Gly
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NM_006516.4:c.1208C>G
MANE Select
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NP_006507.2:p.Ala403Gly
|
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