| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001288629.1 | 3075 | Missense Mutation | ACG,ATG | T940M | NP_001275558.1 |
| NM_001288630.1 | 3075 | Intron | NP_001275559.1 | ||
| NM_004440.3 | 3075 | Missense Mutation | ACG,ATG | T945M | NP_004431.1 |
| XM_005248669.2 | 3075 | Missense Mutation | ACG,ATG | T941M | XP_005248726.1 |
| XM_005248671.2 | 3075 | Intron | XP_005248728.1 | ||
| XM_017010365.1 | 3075 | Missense Mutation | ACG,ATG | T936M | XP_016865854.1 |
| XM_017010366.1 | 3075 | Intron | XP_016865855.1 |