| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020208.3 | 2179 | Missense Mutation | CGT,TGT | R581C | NP_064593.1 |
| NM_022405.3 | 2179 | Missense Mutation | CGT,TGT | R544C | NP_071800.1 |
| XM_011533847.2 | 2179 | Missense Mutation | CGT,TGT | R482C | XP_011532149.1 |
| XM_011533848.2 | 2179 | Intron | XP_011532150.1 |