| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020737.2 | 3249 | Missense Mutation | GCC,GTC | A613V | NP_065788.1 |
| XM_011514761.2 | 3249 | Missense Mutation | GCC,GTC | A613V | XP_011513063.1 |
| XM_011514762.2 | 3249 | Missense Mutation | GCC,GTC | A613V | XP_011513064.1 |
| XM_017011110.1 | 3249 | Missense Mutation | GCC,GTC | A613V | XP_016866599.1 |
| XM_017011111.1 | 3249 | Intron | XP_016866600.1 |