| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001304803.1 | 1516 | UTR 5 | NP_001291732.1 | ||
| NM_021947.2 | 1516 | Missense Mutation | CCG,CTG | P76L | NP_068766.1 |
| XM_006721565.3 | 1516 | Missense Mutation | CCG,CTG | P76L | XP_006721628.1 |
| XM_006721566.3 | 1516 | Missense Mutation | CCG,CTG | P76L | XP_006721629.1 |
| XM_011523974.2 | 1516 | Missense Mutation | CCG,CTG | P76L | XP_011522276.1 |