| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_173482.2 | 362 | Missense Mutation | CAG,CCG | Q88P | NP_775753.2 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001272087.1 | 362 | Intron | NP_001259016.1 | ||
| NM_001272088.1 | 362 | Intron | NP_001259017.1 | ||
| NM_005071.2 | 362 | Intron | NP_005062.1 | ||
| XM_006722842.1 | 362 | Intron | XP_006722905.1 | ||
| XM_006722844.1 | 362 | Intron | XP_006722907.1 | ||
| XM_017027152.1 | 362 | Intron | XP_016882641.1 |