ENST00000330062.8:c.556G>A
MANE Select
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ENSP00000331897.4:p.Ala186Thr
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ENST00000330062.7:c.556G>A
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ENSP00000331897.3:p.Ala186Thr
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ENST00000540499.2:c.400G>A
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ENSP00000446147.2:p.Ala134Thr
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ENST00000559482.5:c.229G>A
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ENSP00000453016.1:p.Ala77Thr
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ENST00000560061.1:c.*181G>A
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ENSP00000453254.1:n.*181G>A
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NM_001289910.1:c.400G>A , LRG_611t1:c.400G>A
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NP_001276839.1:p.Ala134Thr
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NM_001290114.1:c.166G>A
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NP_001277043.1:p.Ala56Thr
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NM_002168.3:c.556G>A , LRG_611t2:c.556G>A
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NP_002159.2:p.Ala186Thr
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NM_001290114.2:c.166G>A
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NP_001277043.1:p.Ala56Thr
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NM_002168.4:c.556G>A
MANE Select
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NP_002159.2:p.Ala186Thr
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