| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033564.2 | 111 | Intron | NP_001028736.1 | ||
| XM_017011174.1 | 111 | Intron | XP_016866663.1 | ||
| XM_017011175.1 | 111 | Intron | XP_016866664.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016262.4 | 111 | Missense Mutation | CGC,TGC | R18C | NP_057346.1 |
| XM_011535875.2 | 111 | UTR 5 | XP_011534177.1 | ||
| XM_017010918.1 | 111 | UTR 5 | XP_016866407.1 |