| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009613.2 | 89 | Intron | NP_001009613.1 | ||
| XM_017029543.1 | 89 | Missense Mutation | AGG,ATG | R1M | XP_016885032.1 |
| XM_017029544.1 | 89 | Missense Mutation | AGG,ATG | R1M | XP_016885033.1 |