| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178564.3 | 1117 | Missense Mutation | CGC,CTC | R326L | NP_848659.2 |
| XM_017013378.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868867.1 |
| XM_017013379.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868868.1 |
| XM_017013380.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868869.1 |
| XM_017013381.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868870.1 |
| XM_017013382.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868871.1 |
| XM_017013383.1 | 1117 | Missense Mutation | CGC,CTC | R326L | XP_016868872.1 |