| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013268.2 | 305 | Missense Mutation | CTT,TTT | L89F | NP_037400.1 |
| XM_011526874.2 | 305 | Missense Mutation | CTT,TTT | L82F | XP_011525176.1 |
| XM_017026715.1 | 305 | Missense Mutation | CTT,TTT | L120F | XP_016882204.1 |