Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003223.2 | 1072 | Missense Mutation | CCC,GCC | P228A | NP_003214.1 |
XM_011522633.2 | 1072 | Missense Mutation | CCC,GCC | P215A | XP_011520935.1 |
XM_011522635.2 | 1072 | Missense Mutation | CCC,GCC | P168A | XP_011520937.1 |