| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001243077.1 | 262 | Missense Mutation | ATT,GTT | I14V | NP_001230006.1 |
| NM_001243078.1 | 262 | Missense Mutation | ATT,GTT | I14V | NP_001230007.1 |
| NM_006139.3 | 262 | Missense Mutation | ATT,GTT | I14V | NP_006130.1 |
| XM_011512194.2 | 262 | Intron | XP_011510496.1 | ||
| XM_011512195.2 | 262 | Intron | XP_011510497.1 | ||
| XM_011512197.2 | 262 | Missense Mutation | ATT,GTT | I14V | XP_011510499.1 |