Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135163.1 | 1760 | Intron | NP_001128635.1 | ||
NM_052884.2 | 1760 | Intron | NP_443116.2 | ||
XM_005258476.3 | 1760 | Silent Mutation | CGC,CGT | R576R | XP_005258533.2 |
XM_005258477.3 | 1760 | Intron | XP_005258534.2 |