Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001013355.1 | 364 | Missense Mutation | CGC,TGC | R122C | NP_001013373.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004693.1 | 364 | Intron | NP_001004693.1 | ||
XM_017000273.1 | 364 | Intron | XP_016855762.1 |