ENST00000330062.8:c.667A>C
MANE Select
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ENSP00000331897.4:p.Asn223His
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ENST00000330062.7:c.667A>C
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ENSP00000331897.3:p.Asn223His
|
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ENST00000540499.2:c.511A>C
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ENSP00000446147.2:p.Asn171His
|
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ENST00000559482.5:c.340A>C
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ENSP00000453016.1:p.Asn114His
|
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ENST00000560061.1:c.*292A>C
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ENSP00000453254.1:n.*292A>C
|
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NM_001289910.1:c.511A>C , LRG_611t1:c.511A>C
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NP_001276839.1:p.Asn171His
|
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NM_001290114.1:c.277A>C
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NP_001277043.1:p.Asn93His
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NM_002168.3:c.667A>C , LRG_611t2:c.667A>C
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NP_002159.2:p.Asn223His
|
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NM_001290114.2:c.277A>C
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NP_001277043.1:p.Asn93His
|
|
NM_002168.4:c.667A>C
MANE Select
|
NP_002159.2:p.Asn223His
|
|