ENST00000436784.7:c.1492G>T
MANE Select
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ENSP00000389175.2:p.Gly498Cys
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ENST00000436784.6:c.1492G>T
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ENSP00000389175.2:p.Gly498Cys
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ENST00000461183.5:c.764G>T
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ENSP00000417264.1:p.Gly255Val
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ENST00000471180.5:c.635G>T
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ENSP00000417526.1:p.Gly212Val
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ENST00000473032.5:c.530G>T
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ENSP00000418951.1:p.Gly177Val
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ENST00000486393.5:c.*855G>T
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ENSP00000419868.1:n.*855G>T
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ENST00000489173.1:n.1786G>T
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NM_145262.3:c.1492G>T
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NP_660305.2:p.Gly498Cys
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NR_026699.1:n.1590G>T
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NR_026700.1:n.696G>T
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NR_026701.1:n.1588G>T
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NR_026702.1:n.626G>T
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XM_005264878.2:c.*611G>T
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XP_005264935.1:n.*611G>T
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XR_245095.2:n.2743G>T
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XM_017005730.1:c.1111G>T
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XP_016861219.1:p.Gly371Cys
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XM_024453351.1:c.1492G>T
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XP_024309119.1:p.Gly498Cys
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XM_024453352.1:c.*611G>T
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XP_024309120.1:n.*611G>T
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XR_001740022.2:n.3394G>T
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XR_001740023.2:n.2918G>T
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XR_245095.4:n.2744G>T
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NM_145262.4:c.1492G>T
MANE Select
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NP_660305.2:p.Gly498Cys
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NR_026699.2:n.1582G>T
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NR_026700.2:n.688G>T
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NR_026701.2:n.1580G>T
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NR_026702.2:n.618G>T
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NM_001144951.2:c.*611G>T
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NP_001138423.1:n.*611G>T
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