| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289986.1 | 1085 | Intron | NP_001276915.1 | ||
| NM_017858.2 | 1085 | Intron | NP_060328.2 | ||
| XM_005254521.2 | 1085 | Missense Mutation | TTA,TTT | L272F | XP_005254578.1 |
| XM_005254522.4 | 1085 | Missense Mutation | TTA,TTT | L272F | XP_005254579.1 |
| XM_006720594.3 | 1085 | Missense Mutation | TTA,TTT | L272F | XP_006720657.1 |
| XM_011521743.1 | 1085 | Missense Mutation | TTA,TTT | L272F | XP_011520045.1 |
| XM_017022390.1 | 1085 | Missense Mutation | TTA,TTT | L272F | XP_016877879.1 |
| XM_017022391.1 | 1085 | Intron | XP_016877880.1 |