Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001243225.1 | 1855 | Intron | NP_001230154.1 | ||
NM_001282327.1 | 1855 | Missense Mutation | ATT,GTT | I296V | NP_001269256.1 |
NM_001282328.1 | 1855 | Missense Mutation | ATT,GTT | I296V | NP_001269257.1 |
NM_014303.3 | 1855 | Intron | NP_055118.1 | ||
XM_006724173.1 | 1855 | Missense Mutation | ATT,GTT | I435V | XP_006724236.1 |
XM_017028678.1 | 1855 | Missense Mutation | ATT,GTT | I296V | XP_016884167.1 |