ENST00000402696.9:c.1754G>T
MANE Select
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ENSP00000385834.3:p.Gly585Val
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ENST00000402696.7:c.1754G>T
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ENSP00000385834.3:p.Gly585Val
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ENST00000461695.1:c.485G>T
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ENST00000467842.1:n.2748G>T
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NM_001063.3:c.1754G>T
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NP_001054.1:p.Gly585Val
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XM_011513100.1:c.1754G>T
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XP_011511402.1:p.Gly585Val
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NM_001354703.1:c.1622G>T
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NP_001341632.1:p.Gly541Val
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NM_001354704.1:c.1373G>T
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NP_001341633.1:p.Gly458Val
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NM_001063.4:c.1754G>T
MANE Select
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NP_001054.2:p.Gly585Val
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NM_001354703.2:c.1622G>T
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NP_001341632.2:p.Gly541Val
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NM_001354704.2:c.1373G>T
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NP_001341633.2:p.Gly458Val
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