| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001318766.1 | 195 | UTR 5 | NP_001305695.1 | ||
| NM_033388.1 | 195 | Missense Mutation | CCG,CTG | P59L | NP_203746.1 |
| XM_005274376.4 | 195 | Missense Mutation | CCG,CTG | P59L | XP_005274433.1 |
| XM_006718732.2 | 195 | Missense Mutation | CCG,CTG | P59L | XP_006718795.1 |
| XM_006718733.3 | 195 | Missense Mutation | CCG,CTG | P59L | XP_006718796.1 |
| XM_006718734.2 | 195 | Intron | XP_006718797.1 | ||
| XM_011545332.1 | 195 | Missense Mutation | CCG,CTG | P59L | XP_011543634.1 |
| XM_011545333.1 | 195 | UTR 5 | XP_011543635.1 | ||
| XM_011545334.1 | 195 | UTR 5 | XP_011543636.1 |