| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001284263.1 | 456 | Missense Mutation | CGT,TGT | R76C | NP_001271192.1 |
| NM_001284264.1 | 456 | Intron | NP_001271193.1 | ||
| NM_001284265.1 | 456 | UTR 5 | NP_001271194.1 | ||
| NM_173510.3 | 456 | Missense Mutation | CGT,TGT | R94C | NP_775781.1 |