Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271661.1 | 384 | Missense Mutation | ATT,GTT | I79V | NP_001258590.1 |
NM_001271662.1 | 384 | Missense Mutation | ATT,GTT | I79V | NP_001258591.1 |
NM_004263.4 | 384 | Missense Mutation | ATT,GTT | I79V | NP_004254.2 |
XM_011532475.2 | 384 | Missense Mutation | ATT,GTT | I79V | XP_011530777.1 |
XM_011532476.2 | 384 | Missense Mutation | ATT,GTT | I79V | XP_011530778.1 |
XM_011532477.2 | 384 | Missense Mutation | ATT,GTT | I79V | XP_011530779.1 |
XM_017003172.1 | 384 | Intron | XP_016858661.1 | ||
XM_017003173.1 | 384 | Intron | XP_016858662.1 | ||
XM_017003174.1 | 384 | Intron | XP_016858663.1 |