ENST00000367698.4:c.887C>T
MANE Select
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ENSP00000356671.3:p.Ala296Val
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ENST00000367698.3:c.887C>T
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ENSP00000356671.3:p.Ala296Val
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ENST00000487183.1:n.538C>T
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ENST00000617423.4:c.559+2046C>T
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ENSP00000478688.1:n.559+2046C>T
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NM_000488.3:c.887C>T , LRG_577t1:c.887C>T
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NP_000479.1:p.Ala296Val
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XM_005245198.2:c.743C>T
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XP_005245255.1:p.Ala248Val
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NM_001365052.1:c.743C>T
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NP_001351981.1:p.Ala248Val
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NM_000488.4:c.887C>T
MANE Select
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NP_000479.1:p.Ala296Val
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NM_001365052.2:c.743C>T
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NP_001351981.1:p.Ala248Val
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NM_001386302.1:c.1010C>T
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NP_001373231.1:p.Ala337Val
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NM_001386303.1:c.968C>T
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NP_001373232.1:p.Ala323Val
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NM_001386304.1:c.866C>T
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NP_001373233.1:p.Ala289Val
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NM_001386305.1:c.830C>T
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NP_001373234.1:p.Ala277Val
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NM_001386306.1:c.671C>T
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NP_001373235.1:p.Ala224Val
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