| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001308263.1 | 426 | Missense Mutation | TGT,TTT | C62F | NP_001295192.1 |
| NM_003799.2 | 426 | Missense Mutation | TGT,TTT | C62F | NP_003790.1 |
| XM_005258162.1 | 426 | Missense Mutation | TGT,TTT | C62F | XP_005258219.1 |
| XM_011525749.1 | 426 | Missense Mutation | TGT,TTT | C62F | XP_011524051.1 |
| XM_011525750.2 | 426 | Missense Mutation | TGT,TTT | C62F | XP_011524052.1 |
| XM_011525751.1 | 426 | Missense Mutation | TGT,TTT | C62F | XP_011524053.1 |
| XM_011525753.1 | 426 | Intron | XP_011524055.1 | ||
| XM_017026061.1 | 426 | Missense Mutation | TGT,TTT | C62F | XP_016881550.1 |