| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001005340.1 | 662 | Missense Mutation | CTC,TTC | L4F | NP_001005340.1 |
| NM_002510.2 | 662 | Missense Mutation | CTC,TTC | L4F | NP_002501.1 |
| XM_005249578.2 | 662 | Missense Mutation | CTC,TTC | L4F | XP_005249635.1 |
| XM_017011676.1 | 662 | Missense Mutation | CTC,TTC | L4F | XP_016867165.1 |
| XM_017011677.1 | 662 | Missense Mutation | CTC,TTC | L4F | XP_016867166.1 |
| XM_017011678.1 | 662 | Missense Mutation | CTC,TTC | L4F | XP_016867167.1 |