| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016217.2 | 922 | Missense Mutation | AGG,GGG | R213G | NP_057301.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153235.3 | 922 | Intron | NP_694967.3 | ||
| XM_005266836.1 | 922 | Intron | XP_005266893.1 | ||
| XM_011535505.2 | 922 | Intron | XP_011533807.1 | ||
| XM_011535506.2 | 922 | Intron | XP_011533808.1 | ||
| XM_017010322.1 | 922 | Intron | XP_016865811.1 |