| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243077.1 | 257 | Missense Mutation | CCT,CTT | P12L | NP_001230006.1 |
| NM_001243078.1 | 257 | Missense Mutation | CCT,CTT | P12L | NP_001230007.1 |
| NM_006139.3 | 257 | Missense Mutation | CCT,CTT | P12L | NP_006130.1 |
| XM_011512194.2 | 257 | Intron | XP_011510496.1 | ||
| XM_011512195.2 | 257 | Intron | XP_011510497.1 | ||
| XM_011512197.2 | 257 | Missense Mutation | CCT,CTT | P12L | XP_011510499.1 |