| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039577.3 | 1355 | Intron | NP_001034666.1 | ||
| NM_001320153.1 | 1355 | Missense Mutation | CCG,CTG | P258L | NP_001307082.1 |
| NM_001320155.1 | 1355 | Missense Mutation | CCG,CTG | P258L | NP_001307084.1 |
| NM_030937.4 | 1355 | Missense Mutation | CCG,CTG | P480L | NP_112199.2 |
| XM_011542216.2 | 1355 | Missense Mutation | CCG,CTG | P513L | XP_011540518.1 |
| XM_011542219.2 | 1355 | Missense Mutation | CCG,CTG | P349L | XP_011540521.1 |
| XM_011542221.2 | 1355 | Missense Mutation | CCG,CTG | P258L | XP_011540523.1 |
| XM_017002420.1 | 1355 | Missense Mutation | CCG,CTG | P358L | XP_016857909.1 |
| XM_017002421.1 | 1355 | Missense Mutation | CCG,CTG | P349L | XP_016857910.1 |
| XM_017002422.1 | 1355 | Missense Mutation | CCG,CTG | P258L | XP_016857911.1 |
| XM_017002423.1 | 1355 | Intron | XP_016857912.1 |