| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003604.2 | 3899 | Missense Mutation | CGC,CTC | R1220L | NP_003595.1 |
| XM_005262220.2 | 3899 | Missense Mutation | CGC,CTC | R1220L | XP_005262277.1 |
| XM_006724713.3 | 3899 | Missense Mutation | CGC,CTC | R1220L | XP_006724776.1 |
| XM_011531061.1 | 3899 | Missense Mutation | CGC,CTC | R1220L | XP_011529363.1 |