| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001134470.1 | 1069 | Intron | NP_001127942.1 | ||
| NM_173552.3 | 1069 | Silent Mutation | CGC,CGT | R178R | NP_775823.1 |
| XM_011512543.2 | 1069 | Silent Mutation | CGC,CGT | R178R | XP_011510845.1 |
| XM_017005869.1 | 1069 | Intron | XP_016861358.1 |