| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_033054.2 | 2203 | Missense Mutation | CCC,CTC | P767L | NP_149043.2 |
| XM_017012503.1 | 2203 | Missense Mutation | CCC,CTC | P652L | XP_016867992.1 |
| XM_017012504.1 | 2203 | Missense Mutation | CCC,CTC | P529L | XP_016867993.1 |