ENST00000330062.8:c.565G>A
MANE Select
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ENSP00000331897.4:p.Ala189Thr
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ENST00000330062.7:c.565G>A
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ENSP00000331897.3:p.Ala189Thr
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ENST00000540499.2:c.409G>A
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ENSP00000446147.2:p.Ala137Thr
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ENST00000559482.5:c.238G>A
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ENSP00000453016.1:p.Ala80Thr
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ENST00000560061.1:c.*190G>A
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ENSP00000453254.1:n.*190G>A
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NM_001289910.1:c.409G>A , LRG_611t1:c.409G>A
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NP_001276839.1:p.Ala137Thr
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NM_001290114.1:c.175G>A
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NP_001277043.1:p.Ala59Thr
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NM_002168.3:c.565G>A , LRG_611t2:c.565G>A
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NP_002159.2:p.Ala189Thr
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NM_001290114.2:c.175G>A
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NP_001277043.1:p.Ala59Thr
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NM_002168.4:c.565G>A
MANE Select
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NP_002159.2:p.Ala189Thr
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