Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006062.2 | 2179 | Missense Mutation | CCC,TCC | P144S | NP_006053.2 |
XM_006711918.3 | 2179 | Missense Mutation | CCC,TCC | P92S | XP_006711981.1 |
XM_017003163.1 | 2179 | Missense Mutation | CCC,TCC | P156S | XP_016858652.1 |