| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001184767.1 | 1826 | Missense Mutation | CCC,TCC | P558S | NP_001171696.1 |
| NM_153346.4 | 1826 | Missense Mutation | CCC,TCC | P649S | NP_699177.2 |
| XM_011545447.1 | 1826 | Missense Mutation | CCC,TCC | P663S | XP_011543749.1 |
| XM_017029266.1 | 1826 | Missense Mutation | CCC,TCC | P621S | XP_016884755.1 |
| XM_017029267.1 | 1826 | Missense Mutation | CCC,TCC | P663S | XP_016884756.1 |