| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003285.2 | 4189 | Missense Mutation | CCC,CTC | P1342L | NP_003276.3 |
| XM_011509949.2 | 4189 | Missense Mutation | CCC,CTC | P1183L | XP_011508251.1 |
| XM_017002218.1 | 4189 | Missense Mutation | CCC,CTC | P1342L | XP_016857707.1 |
| XM_017002219.1 | 4189 | Missense Mutation | CCC,CTC | P1342L | XP_016857708.1 |