Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286829.1 | 1298 | Missense Mutation | ACC,GCC | T468A | NP_001273758.1 |
NM_145201.5 | 1298 | Missense Mutation | ACC,GCC | T468A | NP_660202.3 |
XM_017013975.1 | 1298 | Missense Mutation | ACC,GCC | T541A | XP_016869464.1 |
XM_017013976.1 | 1298 | Missense Mutation | ACC,GCC | T541A | XP_016869465.1 |
XM_017013977.1 | 1298 | Missense Mutation | ACC,GCC | T441A | XP_016869466.1 |
XM_017013978.1 | 1298 | Intron | XP_016869467.1 | ||
XM_017013979.1 | 1298 | Missense Mutation | ACC,GCC | T240A | XP_016869468.1 |
XM_017013980.1 | 1298 | Missense Mutation | ACC,GCC | T240A | XP_016869469.1 |