| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_021969.2 | 486 | Missense Mutation | ACA,ATA | T117I | NP_068804.1 |
| XM_011542297.2 | 486 | Missense Mutation | ACA,ATA | T117I | XP_011540599.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_006600.3 | 486 | Intron | NP_006591.1 | ||
| XM_011540529.1 | 486 | Intron | XP_011538831.1 | ||
| XM_011540530.1 | 486 | Intron | XP_011538832.1 | ||
| XM_017000094.1 | 486 | Intron | XP_016855583.1 | ||
| XM_017000095.1 | 486 | Intron | XP_016855584.1 | ||
| XM_017000096.1 | 486 | Intron | XP_016855585.1 |