| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001126335.1 | 1562 | Missense Mutation | CCG,CTG | P482L | NP_001119807.1 |
| NM_001243036.1 | 1562 | Missense Mutation | CCG,CTG | P482L | NP_001229965.1 |
| NM_014270.4 | 1562 | Missense Mutation | CCG,CTG | P482L | NP_055085.1 |
| XM_006722992.1 | 1562 | Missense Mutation | CCG,CTG | P255L | XP_006723055.1 |
| XM_011526402.2 | 1562 | Missense Mutation | CCG,CTG | P482L | XP_011524704.1 |
| XM_017026230.1 | 1562 | Missense Mutation | CCG,CTG | P394L | XP_016881719.1 |