| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001010844.3 | 362 | Missense Mutation | CGT,TGT | R91C | NP_001010844.1 |
| XM_006715336.3 | 362 | Missense Mutation | CGT,TGT | R91C | XP_006715399.1 |
| XM_011535447.1 | 362 | Missense Mutation | CGT,TGT | R91C | XP_011533749.1 |
| XM_011535448.2 | 362 | Missense Mutation | CGT,TGT | R91C | XP_011533750.1 |
| XM_017010264.1 | 362 | Intron | XP_016865753.1 | ||
| XM_017010265.1 | 362 | Missense Mutation | CGT,TGT | R91C | XP_016865754.1 |