| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278657.1 | 1240 | Missense Mutation | CGC,TGC | R396C | NP_001265586.1 |
| NM_032311.4 | 1240 | Missense Mutation | CGC,TGC | R379C | NP_115687.2 |
| NM_178136.2 | 1240 | Missense Mutation | CGC,TGC | R350C | NP_835237.1 |
| XM_011530457.1 | 1240 | UTR 3 | XP_011528759.1 | ||
| XM_017029010.1 | 1240 | UTR 3 | XP_016884499.1 | ||
| XM_017029011.1 | 1240 | Intron | XP_016884500.1 |