| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300913.1 | 1502 | Intron | NP_001287842.1 | ||
| NM_022338.3 | 1502 | Missense Mutation | CGT,GGT | R354G | NP_071733.1 |
| XM_005274053.3 | 1502 | Missense Mutation | CGT,GGT | R354G | XP_005274110.1 |
| XM_011545103.2 | 1502 | Missense Mutation | CGT,GGT | R322G | XP_011543405.1 |