Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099439.1 | 3042 | Missense Mutation | ACC,GCC | T986A | NP_001092909.1 |
NM_173641.2 | 3042 | Intron | NP_775912.2 | ||
XM_017001080.1 | 3042 | Missense Mutation | ACC,GCC | T589A | XP_016856569.1 |
XM_017001081.1 | 3042 | UTR 3 | XP_016856570.1 |