Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005018.2 | 857 | Missense Mutation | CGC,TGC | R264C | NP_005009.2 |
XM_006712573.2 | 857 | Intron | XP_006712636.1 | ||
XM_017004293.1 | 857 | Missense Mutation | CGC,TGC | R263C | XP_016859782.1 |