ENST00000237596.7:c.1126G>T
MANE Select
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ENSP00000237596.2:p.Gly376Cys
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ENST00000237596.6:c.1126G>T
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ENSP00000237596.2:p.Gly376Cys
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ENST00000506367.1:n.573G>T
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ENST00000508588.5:c.-392G>T
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ENSP00000427131.1:n.-392G>T
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NM_000297.3:c.1126G>T
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NP_000288.1:p.Gly376Cys
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XM_011532028.1:c.1095-3378G>T
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XP_011530330.1:n.1095-3378G>T
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XM_011532029.1:c.406G>T
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XP_011530331.1:p.Gly136Cys
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XM_011532030.1:c.286G>T
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XP_011530332.1:p.Gly96Cys
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XR_244632.2:n.1221G>T
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NR_156488.1:n.1213G>T
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XM_011532028.2:c.1095-3378G>T
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XP_011530330.1:n.1095-3378G>T
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XM_011532030.2:c.286G>T
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XP_011530332.1:p.Gly96Cys
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NM_000297.4:c.1126G>T
MANE Select
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NP_000288.1:p.Gly376Cys
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NR_156488.2:n.1225G>T
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