ENST00000285021.12:c.1810G>T
MANE Select
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ENSP00000285021.8:p.Ala604Ser
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ENST00000285021.11:c.1810G>T
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ENSP00000285021.7:p.Ala604Ser
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ENST00000476581.6:c.*1263G>T
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ENSP00000424548.1:n.*1263G>T
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NM_004628.4:c.1810G>T , LRG_472t1:c.1810G>T
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NP_004619.3:p.Ala604Ser
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NR_027299.1:n.1790G>T
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|
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XM_011534092.1:c.1810G>T
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XP_011532394.1:p.Ala604Ser
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XM_011534093.1:c.1810G>T
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XP_011532395.1:p.Ala604Ser
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NM_001354726.1:c.1231G>T
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NP_001341655.1:p.Ala411Ser
|
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NM_001354727.1:c.1810G>T
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NP_001341656.1:p.Ala604Ser
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NM_001354729.1:c.1792G>T
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NP_001341658.1:p.Ala598Ser
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NM_001354730.1:c.1626+184G>T
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NP_001341659.1:n.1626+184G>T
|
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NR_148950.1:n.1914G>T
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|
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NR_148951.1:n.1790G>T
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|
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XR_001740256.2:n.1843G>T
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|
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XR_002959580.1:n.1843G>T
|
|
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XR_002959581.1:n.1843G>T
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NM_001354727.2:c.1810G>T
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NP_001341656.1:p.Ala604Ser
|
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NM_004628.5:c.1810G>T
MANE Select
|
NP_004619.3:p.Ala604Ser
|
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NR_148950.2:n.1843G>T
|
|
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NR_148951.2:n.1719G>T
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|
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NM_001354726.2:c.1231G>T
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NP_001341655.1:p.Ala411Ser
|
|
NM_001354729.2:c.1792G>T
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NP_001341658.1:p.Ala598Ser
|
|
NM_001354730.2:c.1626+184G>T
|
NP_001341659.1:n.1626+184G>T
|
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