ENST00000285021.12:c.2313T>G
MANE Select
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ENSP00000285021.8:p.Cys771Trp
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ENST00000285021.11:c.2313T>G
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ENSP00000285021.7:p.Cys771Trp
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ENST00000427795.2:n.178T>G
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|
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ENST00000476581.6:c.*1766T>G
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ENSP00000424548.1:n.*1766T>G
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NM_004628.4:c.2313T>G , LRG_472t1:c.2313T>G
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NP_004619.3:p.Cys771Trp
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NR_027299.1:n.2293T>G
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|
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XM_011534092.1:c.2313T>G
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XP_011532394.1:p.Cys771Trp
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NM_001354726.1:c.1734T>G
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NP_001341655.1:p.Cys578Trp
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NM_001354727.1:c.2307T>G
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NP_001341656.1:p.Cys769Trp
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NM_001354729.1:c.2295T>G
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NP_001341658.1:p.Cys765Trp
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NM_001354730.1:c.2067T>G
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NP_001341659.1:p.Cys689Trp
|
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NR_148950.1:n.2256T>G
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|
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NR_148951.1:n.2132T>G
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|
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XR_001740256.2:n.2346T>G
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|
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XR_002959580.1:n.2346T>G
|
|
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XR_002959581.1:n.3963T>G
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|
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NM_001354727.2:c.2307T>G
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NP_001341656.1:p.Cys769Trp
|
|
NM_004628.5:c.2313T>G
MANE Select
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NP_004619.3:p.Cys771Trp
|
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NR_148950.2:n.2185T>G
|
|
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NR_148951.2:n.2061T>G
|
|
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NM_001354726.2:c.1734T>G
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NP_001341655.1:p.Cys578Trp
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|
NM_001354729.2:c.2295T>G
|
NP_001341658.1:p.Cys765Trp
|
|
NM_001354730.2:c.2067T>G
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NP_001341659.1:p.Cys689Trp
|
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