ENST00000330062.8:c.677A>T
MANE Select
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ENSP00000331897.4:p.Glu226Val
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ENST00000330062.7:c.677A>T
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ENSP00000331897.3:p.Glu226Val
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ENST00000540499.2:c.521A>T
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ENSP00000446147.2:p.Glu174Val
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ENST00000559482.5:c.350A>T
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ENSP00000453016.1:p.Glu117Val
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ENST00000560061.1:c.*302A>T
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ENSP00000453254.1:n.*302A>T
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NM_001289910.1:c.521A>T , LRG_611t1:c.521A>T
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NP_001276839.1:p.Glu174Val
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NM_001290114.1:c.287A>T
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NP_001277043.1:p.Glu96Val
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NM_002168.3:c.677A>T , LRG_611t2:c.677A>T
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NP_002159.2:p.Glu226Val
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NM_001290114.2:c.287A>T
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NP_001277043.1:p.Glu96Val
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NM_002168.4:c.677A>T
MANE Select
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NP_002159.2:p.Glu226Val
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