Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_019849.2 | 1658 | Missense Mutation | CGC,TGC | R410C | NP_062823.1 |
XM_006723284.2 | 1658 | Intron | XP_006723347.1 | ||
XM_011527119.1 | 1658 | Missense Mutation | CGC,TGC | R547C | XP_011525421.1 |
XM_011527120.1 | 1658 | Missense Mutation | CGC,TGC | R520C | XP_011525422.1 |