| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009959.2 | 770 | Missense Mutation | ATT,GTT | I226V | NP_001009959.1 |
| NM_001304344.1 | 770 | Missense Mutation | ATT,GTT | I213V | NP_001291273.1 |
| NM_001304345.1 | 770 | Missense Mutation | ATT,GTT | I213V | NP_001291274.1 |
| NM_001304346.1 | 770 | Missense Mutation | ATT,GTT | I193V | NP_001291275.1 |
| NM_020711.2 | 770 | Missense Mutation | ATT,GTT | I213V | NP_065762.1 |