ENST00000285021.12:c.2309G>T
MANE Select
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ENSP00000285021.8:p.Gly770Val
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ENST00000285021.11:c.2309G>T
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ENSP00000285021.7:p.Gly770Val
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ENST00000427795.2:n.174G>T
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ENST00000476581.6:c.*1762G>T
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ENSP00000424548.1:n.*1762G>T
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NM_004628.4:c.2309G>T , LRG_472t1:c.2309G>T
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NP_004619.3:p.Gly770Val
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NR_027299.1:n.2289G>T
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XM_011534092.1:c.2309G>T
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XP_011532394.1:p.Gly770Val
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NM_001354726.1:c.1730G>T
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NP_001341655.1:p.Gly577Val
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NM_001354727.1:c.2303G>T
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NP_001341656.1:p.Gly768Val
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NM_001354729.1:c.2291G>T
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NP_001341658.1:p.Gly764Val
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NM_001354730.1:c.2063G>T
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NP_001341659.1:p.Gly688Val
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NR_148950.1:n.2252G>T
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NR_148951.1:n.2128G>T
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XR_001740256.2:n.2342G>T
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XR_002959580.1:n.2342G>T
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XR_002959581.1:n.3959G>T
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NM_001354727.2:c.2303G>T
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NP_001341656.1:p.Gly768Val
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NM_004628.5:c.2309G>T
MANE Select
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NP_004619.3:p.Gly770Val
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NR_148950.2:n.2181G>T
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NR_148951.2:n.2057G>T
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NM_001354726.2:c.1730G>T
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NP_001341655.1:p.Gly577Val
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NM_001354729.2:c.2291G>T
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NP_001341658.1:p.Gly764Val
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NM_001354730.2:c.2063G>T
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NP_001341659.1:p.Gly688Val
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