| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001130058.1 | 2217 | Intron | NP_001123530.1 | ||
| NM_001320283.1 | 2217 | Missense Mutation | ATA,GTA | I693V | NP_001307212.1 |
| NM_001320285.1 | 2217 | Intron | NP_001307214.1 | ||
| NM_001320287.1 | 2217 | Intron | NP_001307216.1 | ||
| NM_152697.4 | 2217 | Missense Mutation | ATA,GTA | I699V | NP_689910.2 |
| XM_006710445.3 | 2217 | Missense Mutation | ATA,GTA | I657V | XP_006710508.1 |
| XM_011540986.2 | 2217 | Missense Mutation | ATA,GTA | I657V | XP_011539288.1 |
| XM_011540987.2 | 2217 | Missense Mutation | ATA,GTA | I657V | XP_011539289.1 |
| XM_017000607.1 | 2217 | Missense Mutation | ATA,GTA | I706V | XP_016856096.1 |
| XM_017000608.1 | 2217 | Intron | XP_016856097.1 | ||
| XM_017000609.1 | 2217 | Missense Mutation | ATA,GTA | I699V | XP_016856098.1 |
| XM_017000610.1 | 2217 | Missense Mutation | ATA,GTA | I699V | XP_016856099.1 |
| XM_017000611.1 | 2217 | Missense Mutation | ATA,GTA | I699V | XP_016856100.1 |