ENST00000268125.10:c.649A>G
MANE Select
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ENSP00000268125.5:p.Thr217Ala
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ENST00000268125.9:c.649A>G
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ENSP00000268125.5:p.Thr217Ala
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ENST00000563254.1:c.66A>G
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ENST00000567787.1:c.*227A>G
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ENSP00000457251.1:n.*227A>G
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NM_000326.4:c.649A>G
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NP_000317.1:p.Thr217Ala
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XM_011521870.1:c.649A>G
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XP_011520172.1:p.Thr217Ala
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XM_011521871.1:c.574A>G
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XP_011520173.1:p.Thr192Ala
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XM_011521872.1:c.574A>G
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XP_011520174.1:p.Thr192Ala
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XM_011521870.2:c.649A>G
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XP_011520172.1:p.Thr217Ala
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XM_017022460.1:c.676A>G
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XP_016877949.1:p.Thr226Ala
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NM_000326.5:c.649A>G
MANE Select
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NP_000317.1:p.Thr217Ala
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