Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001307929.1 | 381 | Intron | NP_001294858.1 | ||
NM_006360.5 | 381 | Missense Mutation | CAA,CGA | Q79R | NP_006351.2 |
XM_011519840.2 | 381 | Missense Mutation | CAA,CGA | Q16R | XP_011518142.1 |