| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001037283.1 | 687 | Missense Mutation | CCG,CTG | P102L | NP_001032360.1 |
| NM_003751.3 | 687 | Missense Mutation | CCG,CTG | P102L | NP_003742.2 |
| XM_011515599.1 | 687 | Missense Mutation | CCG,CTG | P102L | XP_011513901.1 |
| XM_011515600.1 | 687 | Missense Mutation | CCG,CTG | P102L | XP_011513902.1 |
| XM_011515601.1 | 687 | Intron | XP_011513903.1 | ||
| XM_017012752.1 | 687 | Missense Mutation | CCG,CTG | P102L | XP_016868241.1 |
| XM_017012753.1 | 687 | Missense Mutation | CCG,CTG | P102L | XP_016868242.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_013321.3 | 687 | Intron | NP_037453.1 | ||
| XM_011515329.2 | 687 | Intron | XP_011513631.1 | ||
| XM_011515330.1 | 687 | Intron | XP_011513632.1 | ||
| XM_017012083.1 | 687 | Intron | XP_016867572.1 | ||
| XM_017012084.1 | 687 | Intron | XP_016867573.1 |