| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_018303.5 | 501 | Intron | NP_060773.3 | ||
| XM_017011018.1 | 501 | Intron | XP_016866507.1 | ||
| XM_017011019.1 | 501 | Intron | XP_016866508.1 | ||
| XM_017011020.1 | 501 | Intron | XP_016866509.1 | ||
| XM_017011021.1 | 501 | Intron | XP_016866510.1 | ||
| XM_017011022.1 | 501 | Intron | XP_016866511.1 | ||
| XM_017011023.1 | 501 | Intron | XP_016866512.1 | ||
| XM_017011024.1 | 501 | Intron | XP_016866513.1 | ||
| XM_017011025.1 | 501 | Intron | XP_016866514.1 | ||
| XM_017011026.1 | 501 | Intron | XP_016866515.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_148959.3 | 501 | Missense Mutation | CGC,TGC | R161C | NP_683762.2 |