| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001256124.1 | 1202 | Missense Mutation | CGC,TGC | R367C | NP_001243053.1 |
| NM_173547.3 | 1202 | Missense Mutation | CGC,TGC | R389C | NP_775818.2 |
| XM_006721760.3 | 1202 | Missense Mutation | CGC,TGC | R402C | XP_006721823.1 |
| XM_006721761.3 | 1202 | Missense Mutation | CGC,TGC | R380C | XP_006721824.1 |
| XM_011524499.2 | 1202 | Intron | XP_011522801.1 | ||
| XM_011524500.2 | 1202 | Intron | XP_011522802.1 | ||
| XM_011524501.2 | 1202 | Intron | XP_011522803.1 | ||
| XM_011524502.2 | 1202 | Intron | XP_011522804.1 | ||
| XM_011524503.2 | 1202 | Intron | XP_011522805.1 | ||
| XM_017024343.1 | 1202 | Intron | XP_016879832.1 | ||
| XM_017024344.1 | 1202 | UTR 3 | XP_016879833.1 |