| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153260.2 | 925 | Intron | NP_694992.2 | ||
| XM_011521423.2 | 925 | UTR 3 | XP_011519725.1 | ||
| XM_011521424.2 | 925 | Intron | XP_011519726.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_003825.3 | 925 | Missense Mutation | CGC,TGC | R142C | NP_003816.2 |
| NM_130798.2 | 925 | Intron | NP_570710.1 | ||
| XM_006720725.2 | 925 | Missense Mutation | CGC,TGC | R153C | XP_006720788.1 |
| XM_017022692.1 | 925 | Missense Mutation | CGC,TGC | R153C | XP_016878181.1 |
| XM_017022693.1 | 925 | Intron | XP_016878182.1 | ||
| XM_017022694.1 | 925 | Intron | XP_016878183.1 |