| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001185059.1 | 5258 | Missense Mutation | ACG,ATG | T1481M | NP_001171988.1 |
| NM_001185074.1 | 5258 | Missense Mutation | ACG,ATG | T1245M | NP_001172003.1 |
| NM_024617.3 | 5258 | Missense Mutation | ACG,ATG | T1481M | NP_078893.2 |
| XM_005252207.3 | 5258 | UTR 3 | XP_005252264.1 | ||
| XM_005252208.2 | 5258 | Intron | XP_005252265.1 | ||
| XM_006717283.1 | 5258 | Missense Mutation | ACG,ATG | T1527M | XP_006717346.1 |
| XM_011519011.2 | 5258 | Intron | XP_011517313.1 | ||
| XM_011519012.2 | 5258 | Intron | XP_011517314.1 | ||
| XM_011519013.2 | 5258 | Intron | XP_011517315.1 | ||
| XM_011519014.2 | 5258 | Intron | XP_011517316.1 | ||
| XM_011519015.1 | 5258 | Intron | XP_011517317.1 | ||
| XM_011519016.1 | 5258 | Intron | XP_011517318.1 | ||
| XM_017015130.1 | 5258 | Missense Mutation | ACG,ATG | T1481M | XP_016870619.1 |
| XM_017015131.1 | 5258 | Missense Mutation | ACG,ATG | T1481M | XP_016870620.1 |
| XM_017015132.1 | 5258 | Missense Mutation | ACG,ATG | T770M | XP_016870621.1 |