ENST00000285021.12:c.2317C>A
MANE Select
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ENSP00000285021.8:p.Gln773Lys
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ENST00000285021.11:c.2317C>A
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ENSP00000285021.7:p.Gln773Lys
|
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ENST00000427795.2:n.182C>A
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|
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ENST00000476581.6:c.*1770C>A
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ENSP00000424548.1:n.*1770C>A
|
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NM_004628.4:c.2317C>A , LRG_472t1:c.2317C>A
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NP_004619.3:p.Gln773Lys
|
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NR_027299.1:n.2297C>A
|
|
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XM_011534092.1:c.2317C>A
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XP_011532394.1:p.Gln773Lys
|
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NM_001354726.1:c.1738C>A
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NP_001341655.1:p.Gln580Lys
|
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NM_001354727.1:c.2311C>A
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NP_001341656.1:p.Gln771Lys
|
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NM_001354729.1:c.2299C>A
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NP_001341658.1:p.Gln767Lys
|
|
NM_001354730.1:c.2071C>A
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NP_001341659.1:p.Gln691Lys
|
|
NR_148950.1:n.2260C>A
|
|
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NR_148951.1:n.2136C>A
|
|
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XR_001740256.2:n.2350C>A
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|
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XR_002959580.1:n.2350C>A
|
|
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XR_002959581.1:n.3967C>A
|
|
|
NM_001354727.2:c.2311C>A
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NP_001341656.1:p.Gln771Lys
|
|
NM_004628.5:c.2317C>A
MANE Select
|
NP_004619.3:p.Gln773Lys
|
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NR_148950.2:n.2189C>A
|
|
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NR_148951.2:n.2065C>A
|
|
|
NM_001354726.2:c.1738C>A
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NP_001341655.1:p.Gln580Lys
|
|
NM_001354729.2:c.2299C>A
|
NP_001341658.1:p.Gln767Lys
|
|
NM_001354730.2:c.2071C>A
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NP_001341659.1:p.Gln691Lys
|
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