| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001172638.1 | 2692 | Missense Mutation | CAA,CGA | Q841R | NP_001166109.1 |
| NM_152283.4 | 2692 | Missense Mutation | CAA,CGA | Q808R | NP_689496.4 |
| XM_017009710.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865199.1 |
| XM_017009711.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865200.1 |
| XM_017009712.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865201.1 |
| XM_017009713.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865202.1 |
| XM_017009714.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865203.1 |
| XM_017009715.1 | 2692 | Missense Mutation | CAA,CGA | Q808R | XP_016865204.1 |
| XM_017009716.1 | 2692 | Intron | XP_016865205.1 | ||
| XM_017009717.1 | 2692 | Missense Mutation | CAA,CGA | Q841R | XP_016865206.1 |
| XM_017009718.1 | 2692 | Intron | XP_016865207.1 | ||
| XM_017009719.1 | 2692 | Intron | XP_016865208.1 | ||
| XM_017009720.1 | 2692 | Intron | XP_016865209.1 | ||
| XM_017009721.1 | 2692 | Intron | XP_016865210.1 |