Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017742.5 | 652 | Missense Mutation | CCC,CGC | P292R | NP_060212.4 |
XM_006722493.3 | 652 | Missense Mutation | CCC,CGC | P212R | XP_006722556.1 |
XM_011526044.1 | 652 | Intron | XP_011524346.1 | ||
XM_017025802.1 | 652 | Missense Mutation | CCC,CGC | P212R | XP_016881291.1 |