Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207395.2 | 210 | Missense Mutation | CGC,TGC | R27C | NP_997278.2 |
XM_005258915.4 | 210 | Missense Mutation | CGC,TGC | R27C | XP_005258972.1 |
XM_005258918.4 | 210 | Missense Mutation | CGC,TGC | R27C | XP_005258975.1 |