Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_145305.2 | 659 | Missense Mutation | ATT,GTT | I184V | NP_660348.2 |
XM_017029340.1 | 659 | Missense Mutation | ATT,GTT | I184V | XP_016884829.1 |
XM_017029341.1 | 659 | Missense Mutation | ATT,GTT | I184V | XP_016884830.1 |