| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000732.4 | 126 | Intron | NP_000723.1 | ||
| NM_001040651.1 | 126 | Intron | NP_001035741.1 | ||
| XM_017018543.1 | 126 | Intron | XP_016874032.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000073.2 | 126 | Missense Mutation | CTT,TTT | L16F | NP_000064.1 |
| XM_005271724.3 | 126 | Missense Mutation | CTT,TTT | L16F | XP_005271781.1 |
| XM_006718941.2 | 126 | Missense Mutation | CTT,TTT | L16F | XP_006719004.1 |