| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130910.1 | 880 | Missense Mutation | CTT,TTT | L211F | NP_001124382.1 |
| NM_003965.4 | 880 | Missense Mutation | CTT,TTT | L199F | NP_003956.2 |
| XM_011534208.1 | 880 | Missense Mutation | CTT,TTT | L199F | XP_011532510.1 |
| XM_011534209.1 | 880 | Missense Mutation | CTT,TTT | L199F | XP_011532511.1 |
| XM_017007436.1 | 880 | Missense Mutation | CTT,TTT | L199F | XP_016862925.1 |