Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015111.1 | 582 | Missense Mutation | CGC,CTC | R112L | NP_055926.1 |
XM_006714834.3 | 582 | Missense Mutation | CGC,CTC | R112L | XP_006714897.1 |
XM_011534473.1 | 582 | Missense Mutation | CGC,CTC | R112L | XP_011532775.1 |
XM_011534474.1 | 582 | Missense Mutation | CGC,CTC | R112L | XP_011532776.1 |