| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000751.2 | 155 | Missense Mutation | CGG,TGG | R43W | NP_000742.1 |
| NM_001256657.1 | 155 | Missense Mutation | CGG,TGG | R43W | NP_001243586.1 |
| NM_001311195.1 | 155 | UTR 5 | NP_001298124.1 | ||
| NM_001311196.1 | 155 | UTR 5 | NP_001298125.1 | ||
| XM_011510524.2 | 155 | UTR 5 | XP_011508826.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195129.1 | 155 | Intron | NP_001182058.1 |