ENST00000398752.11:c.829G>T
MANE Select
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ENSP00000381736.5:p.Ala277Ser
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ENST00000282050.6:c.829G>T
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ENSP00000282050.2:p.Ala277Ser
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ENST00000398752.10:c.829G>T
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ENSP00000381736.5:p.Ala277Ser
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ENST00000586523.1:n.1234G>T
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ENST00000586592.5:c.*892G>T
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ENSP00000466275.3:n.*892G>T
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ENST00000589252.5:c.562G>T
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ENSP00000466975.1:p.Ala188Ser
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ENST00000590156.5:c.*725G>T
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ENSP00000466309.1:n.*725G>T
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ENST00000590665.5:c.763G>T
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ENSP00000467037.1:p.Ala255Ser
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ENST00000592364.5:c.227-399G>T
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ENSP00000468618.1:n.227-399G>T
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ENST00000593152.6:c.679G>T
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ENSP00000465477.2:p.Ala227Ser
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NM_001001935.2:c.679G>T
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NP_001001935.1:p.Ala227Ser
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NM_001001937.1:c.829G>T
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NP_001001937.1:p.Ala277Ser
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NM_001257334.1:c.763G>T
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NP_001244263.1:p.Ala255Ser
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NM_001257335.1:c.679G>T
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NP_001244264.1:p.Ala227Ser
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NM_004046.5:c.829G>T
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NP_004037.1:p.Ala277Ser
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XM_011526018.1:c.679G>T
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XP_011524320.1:p.Ala227Ser
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XM_017025789.1:c.829G>T
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XP_016881278.1:p.Ala277Ser
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NM_004046.6:c.829G>T
MANE Select
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NP_004037.1:p.Ala277Ser
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NM_001001935.3:c.679G>T
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NP_001001935.1:p.Ala227Ser
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NM_001257334.2:c.763G>T
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NP_001244263.1:p.Ala255Ser
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NM_001001937.2:c.829G>T
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NP_001001937.1:p.Ala277Ser
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NM_001257335.2:c.679G>T
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NP_001244264.1:p.Ala227Ser
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