| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001307943.1 | 89 | Missense Mutation | GTT,TTT | V7F | NP_001294872.1 |
| NM_018259.5 | 89 | Missense Mutation | GTT,TTT | V7F | NP_060729.2 |
| XM_005253016.1 | 89 | Missense Mutation | GTT,TTT | V7F | XP_005253073.1 |
| XM_006718263.1 | 89 | Intron | XP_006718326.1 | ||
| XM_011520218.2 | 89 | Missense Mutation | GTT,TTT | V7F | XP_011518520.1 |
| XM_017018010.1 | 89 | Missense Mutation | GTT,TTT | V7F | XP_016873499.1 |