| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003730.4 | 957 | Missense Mutation | CGC,TGC | R184C | NP_003721.2 |
| XM_017011397.1 | 957 | Intron | XP_016866886.1 | ||
| XM_017011398.1 | 957 | Intron | XP_016866887.1 | ||
| XM_017011399.1 | 957 | UTR 3 | XP_016866888.1 |