| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001321355.1 | 1795 | Missense Mutation | CTT,TTT | L479F | NP_001308284.1 |
| NM_001321356.1 | 1795 | Missense Mutation | CTT,TTT | L536F | NP_001308285.1 |
| NM_022103.3 | 1795 | Missense Mutation | CTT,TTT | L536F | NP_071386.3 |
| XM_011527208.1 | 1795 | Missense Mutation | CTT,TTT | L536F | XP_011525510.1 |
| XM_011527209.1 | 1795 | Missense Mutation | CTT,TTT | L536F | XP_011525511.1 |