ENST00000285021.12:c.2336T>A
MANE Select
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ENSP00000285021.8:p.Leu779Gln
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ENST00000285021.11:c.2336T>A
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ENSP00000285021.7:p.Leu779Gln
|
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ENST00000427795.2:n.201T>A
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|
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ENST00000476581.6:c.*1789T>A
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ENSP00000424548.1:n.*1789T>A
|
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NM_004628.4:c.2336T>A , LRG_472t1:c.2336T>A
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NP_004619.3:p.Leu779Gln
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NR_027299.1:n.2316T>A
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|
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XM_011534092.1:c.2336T>A
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XP_011532394.1:p.Leu779Gln
|
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NM_001354726.1:c.1757T>A
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NP_001341655.1:p.Leu586Gln
|
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NM_001354727.1:c.2330T>A
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NP_001341656.1:p.Leu777Gln
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NM_001354729.1:c.2318T>A
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NP_001341658.1:p.Leu773Gln
|
|
NM_001354730.1:c.2090T>A
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NP_001341659.1:p.Leu697Gln
|
|
NR_148950.1:n.2279T>A
|
|
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NR_148951.1:n.2155T>A
|
|
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XR_001740256.2:n.2369T>A
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|
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XR_002959580.1:n.2369T>A
|
|
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XR_002959581.1:n.3986T>A
|
|
|
NM_001354727.2:c.2330T>A
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NP_001341656.1:p.Leu777Gln
|
|
NM_004628.5:c.2336T>A
MANE Select
|
NP_004619.3:p.Leu779Gln
|
|
NR_148950.2:n.2208T>A
|
|
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NR_148951.2:n.2084T>A
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|
|
NM_001354726.2:c.1757T>A
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NP_001341655.1:p.Leu586Gln
|
|
NM_001354729.2:c.2318T>A
|
NP_001341658.1:p.Leu773Gln
|
|
NM_001354730.2:c.2090T>A
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NP_001341659.1:p.Leu697Gln
|
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