| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003272.3 | 449 | Missense Mutation | CTC,TTC | L120F | NP_003263.1 |
| XM_017002209.1 | 449 | Missense Mutation | CTC,TTC | L120F | XP_016857698.1 |
| XM_017002210.1 | 449 | Missense Mutation | CTC,TTC | L120F | XP_016857699.1 |