ENST00000436784.7:c.1493G>C
MANE Select
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ENSP00000389175.2:p.Gly498Ala
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ENST00000436784.6:c.1493G>C
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ENSP00000389175.2:p.Gly498Ala
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ENST00000461183.5:c.765G>C
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ENSP00000417264.1:p.Gly255=
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ENST00000471180.5:c.636G>C
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ENSP00000417526.1:p.Gly212=
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ENST00000473032.5:c.531G>C
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ENSP00000418951.1:p.Gly177=
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ENST00000486393.5:c.*856G>C
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ENSP00000419868.1:n.*856G>C
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ENST00000489173.1:n.1787G>C
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NM_145262.3:c.1493G>C
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NP_660305.2:p.Gly498Ala
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NR_026699.1:n.1591G>C
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NR_026700.1:n.697G>C
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NR_026701.1:n.1589G>C
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NR_026702.1:n.627G>C
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XM_005264878.2:c.*612G>C
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XP_005264935.1:n.*612G>C
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XR_245095.2:n.2744G>C
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XM_017005730.1:c.1112G>C
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XP_016861219.1:p.Gly371Ala
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XM_024453351.1:c.1493G>C
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XP_024309119.1:p.Gly498Ala
|
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XM_024453352.1:c.*612G>C
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XP_024309120.1:n.*612G>C
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XR_001740022.2:n.3395G>C
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XR_001740023.2:n.2919G>C
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XR_245095.4:n.2745G>C
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NM_145262.4:c.1493G>C
MANE Select
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NP_660305.2:p.Gly498Ala
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NR_026699.2:n.1583G>C
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NR_026700.2:n.689G>C
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NR_026701.2:n.1581G>C
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NR_026702.2:n.619G>C
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NM_001144951.2:c.*612G>C
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NP_001138423.1:n.*612G>C
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