ENST00000053867.8:c.1385G>C
MANE Select
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ENSP00000053867.2:p.Gly462Ala
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ENST00000639447.1:c.1137-309G>C
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ENSP00000492014.1:n.1137-309G>C
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ENST00000053867.7:c.1385G>C
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ENSP00000053867.2:p.Gly462Ala
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ENST00000586242.1:c.19G>C
|
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ENST00000586443.1:c.826G>C
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ENST00000589265.5:c.914G>C
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ENSP00000467616.1:p.Gly305Ala
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NM_002087.3:c.1385G>C
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NP_002078.1:p.Gly462Ala
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XM_005257253.1:c.1385G>C
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XP_005257310.1:p.Gly462Ala
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XM_024450730.1:c.1385G>C
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XP_024306498.1:p.Gly462Ala
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NM_002087.4:c.1385G>C
MANE Select
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NP_002078.1:p.Gly462Ala
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