| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001098478.1 | 227 | Missense Mutation | ACG,ATG | T66M | NP_001091948.1 |
| NM_001098479.1 | 227 | Missense Mutation | ACG,ATG | T66M | NP_001091949.1 |
| NM_018950.2 | 227 | Missense Mutation | ACG,ATG | T66M | NP_061823.2 |
| XM_011514564.1 | 227 | Missense Mutation | ACG,ATG | T66M | XP_011512866.1 |
| XM_017010810.1 | 227 | Missense Mutation | ACG,ATG | T66M | XP_016866299.1 |
| XM_017010811.1 | 227 | Missense Mutation | ACG,ATG | T66M | XP_016866300.1 |
| XM_017010812.1 | 227 | Missense Mutation | ACG,ATG | T66M | XP_016866301.1 |
| XM_017010813.1 | 227 | Missense Mutation | ACG,ATG | T66M | XP_016866302.1 |
| XM_017010814.1 | 227 | UTR 5 | XP_016866303.1 | ||
| XM_017010815.1 | 227 | UTR 5 | XP_016866304.1 |