| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001109.4 | 2526 | Silent Mutation | CCA,CCG | P753P | NP_001100.3 |
| NM_001164489.1 | 2526 | Missense Mutation | AGT,GGT | S698G | NP_001157961.1 |
| NM_001164490.1 | 2526 | Silent Mutation | CCA,CCG | P688P | NP_001157962.1 |
| XM_011539117.2 | 2526 | Silent Mutation | CCA,CCG | P818P | XP_011537419.2 |
| XM_017015465.1 | 2526 | Silent Mutation | CCA,CCG | P818P | XP_016870954.1 |
| XM_017015466.1 | 2526 | Intron | XP_016870955.1 |