| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291494.1 | 3598 | Missense Mutation | ACC,GCC | T1012A | NP_001278423.1 |
| NM_003638.2 | 3598 | Missense Mutation | ACC,GCC | T1027A | NP_003629.2 |
| XM_011519752.2 | 3598 | Intron | XP_011518054.1 |