Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308229.1 | 858 | Missense Mutation | CGC,TGC | R275C | NP_001295158.1 |
NM_173657.2 | 858 | Missense Mutation | CGC,TGC | R232C | NP_775928.1 |
XM_005247379.4 | 858 | Intron | XP_005247436.1 | ||
XM_011512710.2 | 858 | Missense Mutation | CGC,TGC | R255C | XP_011511012.1 |
XM_011512711.2 | 858 | Intron | XP_011511013.1 |