| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001287595.1 | 1460 | Missense Mutation | ATT,GTT | I592V | NP_001274524.1 |
| NM_001287596.1 | 1460 | Intron | NP_001274525.1 | ||
| NM_001287597.1 | 1460 | Missense Mutation | CAT,CGT | H467R | NP_001274526.1 |
| NM_006671.5 | 1460 | Missense Mutation | ATT,GTT | I533V | NP_006662.3 |
| XM_011542002.2 | 1460 | Missense Mutation | ATT,GTT | I310V | XP_011540304.1 |