| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001317980.1 | 169 | Missense Mutation | ATG,GTG | M25V | NP_001304909.1 |
| NM_001317981.1 | 169 | Missense Mutation | ATG,GTG | M25V | NP_001304910.1 |
| NM_001317982.1 | 169 | Missense Mutation | ATG,GTG | M25V | NP_001304911.1 |
| NM_016093.3 | 169 | Intron | NP_057177.1 | ||
| XM_005265921.3 | 169 | Missense Mutation | ATG,GTG | M54V | XP_005265978.1 |
| XM_011534565.2 | 169 | Missense Mutation | ATG,GTG | M25V | XP_011532867.1 |
| XM_017009519.1 | 169 | Missense Mutation | ATG,GTG | M25V | XP_016865008.1 |
| XM_017009520.1 | 169 | Intron | XP_016865009.1 |