Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001127464.2 | 1262 | Missense Mutation | CCC,TCC | P357S | NP_001120936.2 |
XM_017023784.1 | 1262 | Missense Mutation | CCC,TCC | P357S | XP_016879273.1 |
XM_017023785.1 | 1262 | Missense Mutation | CCC,TCC | P357S | XP_016879274.1 |