ENST00000330062.8:c.676G>T
MANE Select
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ENSP00000331897.4:p.Glu226Ter
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ENST00000330062.7:c.676G>T
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ENSP00000331897.3:p.Glu226Ter
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ENST00000540499.2:c.520G>T
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ENSP00000446147.2:p.Glu174Ter
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ENST00000559482.5:c.349G>T
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ENSP00000453016.1:p.Glu117Ter
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ENST00000560061.1:c.*301G>T
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ENSP00000453254.1:n.*301G>T
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NM_001289910.1:c.520G>T , LRG_611t1:c.520G>T
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NP_001276839.1:p.Glu174Ter
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NM_001290114.1:c.286G>T
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NP_001277043.1:p.Glu96Ter
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NM_002168.3:c.676G>T , LRG_611t2:c.676G>T
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NP_002159.2:p.Glu226Ter
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NM_001290114.2:c.286G>T
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NP_001277043.1:p.Glu96Ter
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NM_002168.4:c.676G>T
MANE Select
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NP_002159.2:p.Glu226Ter
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