Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005559.3 | 9056 | Missense Mutation | CGT,TGT | R2988C | NP_005550.2 |
XM_011525655.2 | 9056 | Missense Mutation | CGT,TGT | R2998C | XP_011523957.1 |
XM_011525656.2 | 9056 | Missense Mutation | CGT,TGT | R2474C | XP_011523958.1 |
XM_011525657.1 | 9056 | Intron | XP_011523959.1 |