| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001171990.2 | 699 | Missense Mutation | CGT,CTT | R100L | NP_001165461.1 |
| NM_001323018.1 | 699 | Missense Mutation | CGT,CTT | R74L | NP_001309947.1 |
| NM_001323019.1 | 699 | Missense Mutation | CGT,CTT | R100L | NP_001309948.1 |
| NM_001323020.1 | 699 | Missense Mutation | CGT,CTT | R74L | NP_001309949.1 |
| NM_001323022.1 | 699 | UTR 5 | NP_001309951.1 | ||
| NM_153706.3 | 699 | Missense Mutation | CGT,CTT | R100L | NP_714917.2 |
| XM_005248426.4 | 699 | Intron | XP_005248483.1 | ||
| XM_011543139.2 | 699 | Missense Mutation | CGT,CTT | R68L | XP_011541441.1 |
| XM_011543140.2 | 699 | Missense Mutation | CGT,CTT | R24L | XP_011541442.1 |