ENST00000290866.10:c.353G>A
MANE Select
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ENSP00000290866.4:p.Arg118His
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ENST00000290866.9:c.353G>A
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ENSP00000290866.4:p.Arg118His
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ENST00000428043.5:c.353G>A
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ENSP00000397593.2:p.Arg118His
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ENST00000579462.1:n.378G>A
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ENST00000580318.1:n.542G>A
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ENST00000582627.1:c.353G>A
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ENSP00000462280.1:p.Arg118His
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ENST00000582678.5:c.353G>A
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ENSP00000462995.1:p.Arg118His
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ENST00000583336.5:n.387G>A
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ENST00000584529.5:n.387G>A
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NM_000789.3:c.353G>A
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NP_000780.1:p.Arg118His
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XM_005257110.1:c.-103G>A
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XP_005257167.1:n.-103G>A
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NM_000789.4:c.353G>A
MANE Select
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NP_000780.1:p.Arg118His
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NM_001382700.1:c.118G>A
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NP_001369629.1:p.Ala40Thr
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NM_001382701.1:c.-262G>A
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NP_001369630.1:n.-262G>A
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