| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080400.1 | 5800 | Missense Mutation | CGG,CTG | R1280L | NP_001073869.1 |
| XM_006722866.2 | 5800 | Missense Mutation | CGG,CTG | R1295L | XP_006722929.1 |
| XM_006722868.3 | 5800 | Missense Mutation | CGG,CTG | R1294L | XP_006722931.1 |
| XM_011528233.2 | 5800 | Missense Mutation | CGG,CTG | R1355L | XP_011526535.1 |
| XM_017027192.1 | 5800 | Missense Mutation | CGG,CTG | R1356L | XP_016882681.1 |
| XM_017027193.1 | 5800 | Missense Mutation | CGG,CTG | R1356L | XP_016882682.1 |
| XM_017027194.1 | 5800 | Missense Mutation | CGG,CTG | R1356L | XP_016882683.1 |