| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142546.1 | 3500 | Missense Mutation | CCG,CTG | P1039L | NP_001136018.1 |
| NM_033631.3 | 3500 | Missense Mutation | CCG,CTG | P1039L | NP_361013.3 |
| XM_011542090.2 | 3500 | Missense Mutation | CCG,CTG | P1039L | XP_011540392.1 |
| XM_011542091.2 | 3500 | Missense Mutation | CCG,CTG | P1039L | XP_011540393.1 |
| XM_017002252.1 | 3500 | Missense Mutation | CCG,CTG | P1039L | XP_016857741.1 |