Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032272.4 | 926 | Missense Mutation | AAT,AGT | N101S | NP_115648.2 |
XM_017013903.1 | 926 | Missense Mutation | AAT,AGT | N101S | XP_016869392.1 |
XM_017013904.1 | 926 | Intron | XP_016869393.1 |