| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286761.1 | 1777 | Missense Mutation | ACG,ATG | T610M | NP_001273690.1 |
| NM_001286762.1 | 1777 | Nonsense Mutation | CGA,TGA | R559* | NP_001273691.1 |
| NM_001286763.1 | 1777 | Missense Mutation | ACG,ATG | T543M | NP_001273692.1 |
| NM_001286764.1 | 1777 | Missense Mutation | ACG,ATG | T475M | NP_001273693.1 |
| NM_001286765.1 | 1777 | Missense Mutation | ACG,ATG | T453M | NP_001273694.1 |
| NM_001286766.1 | 1777 | Missense Mutation | ACG,ATG | T395M | NP_001273695.1 |
| NM_025113.3 | 1777 | Missense Mutation | ACG,ATG | T610M | NP_079389.2 |