| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001164694.1 | 265 | Missense Mutation | CCC,CTC | P42L | NP_001158166.1 |
| NM_001164695.1 | 265 | Missense Mutation | CCC,CTC | P42L | NP_001158167.1 |
| NM_001318495.1 | 265 | UTR 5 | NP_001305424.1 | ||
| NM_203395.2 | 265 | Missense Mutation | CCC,CTC | P42L | NP_981932.1 |
| XM_006715478.3 | 265 | Missense Mutation | CCC,CTC | P42L | XP_006715541.1 |
| XM_006715479.3 | 265 | Intron | XP_006715542.1 |