| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001198843.1 | 1059 | Intron | NP_001185772.1 | ||
| NM_001198844.1 | 1059 | Intron | NP_001185773.1 | ||
| NM_002896.3 | 1059 | Intron | NP_002887.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286135.1 | 1059 | Intron | NP_001273064.1 | ||
| NM_031492.3 | 1059 | Missense Mutation | CGT,CTT | R308L | NP_113680.1 |
| XM_011545297.2 | 1059 | Missense Mutation | CGT,CTT | R308L | XP_011543599.1 |
| XM_017018402.1 | 1059 | Missense Mutation | CGT,CTT | R308L | XP_016873891.1 |