| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015113.3 | 8902 | Missense Mutation | ACG,ATG | T2925M | NP_055928.3 |
| XM_005256561.2 | 8902 | Missense Mutation | ACG,ATG | T2926M | XP_005256618.1 |
| XM_011523759.2 | 8902 | Intron | XP_011522061.1 | ||
| XM_017024382.1 | 8902 | Missense Mutation | ACG,ATG | T2926M | XP_016879871.1 |
| XM_017024383.1 | 8902 | Missense Mutation | ACG,ATG | T2925M | XP_016879872.1 |
| XM_017024384.1 | 8902 | Missense Mutation | ACG,ATG | T1541M | XP_016879873.1 |