Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_019016.2 | 1205 | Missense Mutation | CAA,CGA | Q491R | NP_061889.2 |
XM_006721739.3 | 1205 | Missense Mutation | CAA,CGA | Q393R | XP_006721802.1 |
XM_011524460.2 | 1205 | Missense Mutation | CAA,CGA | Q388R | XP_011522762.1 |
XM_017024299.1 | 1205 | Intron | XP_016879788.1 |