Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281476.2 | 2755 | Missense Mutation | CAT,CGT | H768R | NP_001268405.1 |
NM_001322046.1 | 2755 | Missense Mutation | CAT,CGT | H811R | NP_001308975.1 |
NM_001322048.1 | 2755 | Missense Mutation | CAT,CGT | H788R | NP_001308977.1 |
NM_001322049.1 | 2755 | Missense Mutation | CAT,CGT | H745R | NP_001308978.1 |
NM_024622.5 | 2755 | Missense Mutation | CAT,CGT | H811R | NP_078898.3 |
XM_006712750.3 | 2755 | Missense Mutation | CAT,CGT | H788R | XP_006712813.1 |
XM_006712751.3 | 2755 | Missense Mutation | CAT,CGT | H491R | XP_006712814.1 |
XM_017004911.1 | 2755 | Missense Mutation | CAT,CGT | H639R | XP_016860400.1 |
XM_017004912.1 | 2755 | Missense Mutation | CAT,CGT | H448R | XP_016860401.1 |