| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001142929.1 | 882 | Intron | NP_001136401.1 | ||
| NM_001142933.1 | 882 | Intron | NP_001136405.1 | ||
| NM_001142934.1 | 882 | Intron | NP_001136406.1 | ||
| NM_020549.4 | 882 | Intron | NP_065574.3 | ||
| NM_020984.3 | 882 | Intron | NP_066264.3 | ||
| NM_020985.3 | 882 | Intron | NP_066265.3 | ||
| NM_020986.3 | 882 | Intron | NP_066266.3 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003055.2 | 882 | Missense Mutation | CGC,TGC | R148C | NP_003046.2 |