| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012643.3 | 1129 | Missense Mutation | ACA,GCA | T348A | NP_001012661.1 |
| XM_017026742.1 | 1129 | Missense Mutation | ACA,GCA | T491A | XP_016882231.1 |
| XM_017026743.1 | 1129 | UTR 3 | XP_016882232.1 |