| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300761.2 | 1668 | Missense Mutation | ATT,TTT | I472F | NP_001287690.1 |
| NM_001317806.1 | 1668 | Missense Mutation | ATT,TTT | I445F | NP_001304735.1 |
| NM_031956.3 | 1668 | Missense Mutation | ATT,TTT | I446F | NP_114162.2 |
| XM_005263270.1 | 1668 | Missense Mutation | ATT,TTT | I463F | XP_005263327.1 |
| XM_006714335.1 | 1668 | Missense Mutation | ATT,TTT | I471F | XP_006714398.1 |
| XM_006714336.1 | 1668 | Missense Mutation | ATT,TTT | I462F | XP_006714399.1 |
| XM_006714339.2 | 1668 | Missense Mutation | ATT,TTT | I410F | XP_006714402.1 |
| XM_011532310.2 | 1668 | Intron | XP_011530612.1 |