| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301060.1 | 1270 | Intron | NP_001287989.1 | ||
| NM_024848.2 | 1270 | Missense Mutation | CCG,CTG | P448L | NP_079124.1 |
| XM_005244798.2 | 1270 | Missense Mutation | CCG,CTG | P424L | XP_005244855.1 |
| XM_011542169.1 | 1270 | Missense Mutation | CCG,CTG | P447L | XP_011540471.1 |
| XM_011542170.2 | 1270 | Intron | XP_011540472.1 | ||
| XM_011542172.2 | 1270 | Intron | XP_011540474.1 | ||
| XM_011542173.2 | 1270 | Intron | XP_011540475.1 | ||
| XM_011542174.2 | 1270 | UTR 3 | XP_011540476.1 | ||
| XM_011542176.1 | 1270 | Missense Mutation | CCG,CTG | P351L | XP_011540478.1 |
| XM_011542177.1 | 1270 | Intron | XP_011540479.1 | ||
| XM_017002365.1 | 1270 | Intron | XP_016857854.1 |