| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001322340.1 | 892 | Intron | NP_001309269.1 | ||
| NM_001322341.1 | 892 | Intron | NP_001309270.1 | ||
| NM_001322342.1 | 892 | Intron | NP_001309271.1 | ||
| NM_001322343.1 | 892 | Intron | NP_001309272.1 | ||
| NM_001322344.1 | 892 | Intron | NP_001309273.1 | ||
| NM_022779.8 | 892 | Intron | NP_073616.6 | ||
| NM_138620.1 | 892 | Intron | NP_619526.1 | ||
| XM_005272207.4 | 892 | Intron | XP_005272264.1 | ||
| XM_006717236.3 | 892 | Intron | XP_006717299.1 | ||
| XM_011518921.2 | 892 | Intron | XP_011517223.1 | ||
| XM_011518922.2 | 892 | Intron | XP_011517224.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012204.3 | 892 | Missense Mutation | CCC,TCC | P110S | NP_036336.2 |
| XM_017015317.1 | 892 | Missense Mutation | CCC,TCC | P110S | XP_016870806.1 |
| XM_017015318.1 | 892 | Missense Mutation | CCC,TCC | P110S | XP_016870807.1 |