| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278182.1 | 1835 | Missense Mutation | ATT,GTT | I491V | NP_001265111.1 |
| NM_001278183.1 | 1835 | Missense Mutation | ATT,GTT | I196V | NP_001265112.1 |
| NM_005442.3 | 1835 | Missense Mutation | ATT,GTT | I472V | NP_005433.2 |
| XM_005265510.3 | 1835 | Intron | XP_005265567.1 |