| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000674.2 | 464 | Missense Mutation | GCC,TCC | A11S | NP_000665.1 |
| NM_001048230.1 | 464 | Missense Mutation | GCC,TCC | A11S | NP_001041695.1 |
| XM_005244901.1 | 464 | UTR 5 | XP_005244958.1 | ||
| XM_005244902.4 | 464 | Intron | XP_005244959.1 | ||
| XM_017000342.1 | 464 | UTR 5 | XP_016855831.1 |