| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001204760.1 | 714 | Missense Mutation | CGG,GGG | R23G | NP_001191689.1 |
| NM_012464.4 | 714 | Missense Mutation | CGG,GGG | R23G | NP_036596.3 |
| XM_011532214.1 | 714 | UTR 5 | XP_011530516.1 | ||
| XM_017008570.1 | 714 | UTR 5 | XP_016864059.1 |