| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000019.3 | 402 | Missense Mutation | ATT,GTT | I115V | NP_000010.1 |
| XM_006718835.3 | 402 | Missense Mutation | ATT,GTT | I25V | XP_006718898.1 |
| XM_017017681.1 | 402 | Missense Mutation | ATT,GTT | I25V | XP_016873170.1 |
| XM_017017682.1 | 402 | Intron | XP_016873171.1 | ||
| XM_017017683.1 | 402 | Intron | XP_016873172.1 |