| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| XM_005264343.3 | 982 | Intron | XP_005264400.1 | ||
| XM_006712026.3 | 982 | Missense Mutation | ACA,GCA | T210A | XP_006712089.1 |
| XM_006712027.3 | 982 | Missense Mutation | ACA,GCA | T210A | XP_006712090.1 |
| XM_011532877.2 | 982 | Missense Mutation | ACA,GCA | T210A | XP_011531179.1 |
| XM_011532878.2 | 982 | Intron | XP_011531180.1 | ||
| XM_011532879.2 | 982 | Missense Mutation | ACA,GCA | T138A | XP_011531181.1 |
| XM_011532880.2 | 982 | Missense Mutation | ACA,GCA | T138A | XP_011531182.1 |
| XM_017004232.1 | 982 | Missense Mutation | ACA,GCA | T210A | XP_016859721.1 |
| XM_017004233.1 | 982 | Missense Mutation | ACA,GCA | T210A | XP_016859722.1 |
| XM_017004234.1 | 982 | Missense Mutation | ACA,GCA | T171A | XP_016859723.1 |
| XM_017004235.1 | 982 | Missense Mutation | ACA,GCA | T171A | XP_016859724.1 |