Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001146094.1 | 587 | Missense Mutation | ACA,GCA | T98A | NP_001139566.1 |
NM_001146095.1 | 587 | Missense Mutation | ACA,GCA | T98A | NP_001139567.1 |
NM_001146096.1 | 587 | Missense Mutation | ACA,GCA | T98A | NP_001139568.1 |
NM_014967.4 | 587 | Missense Mutation | ACA,GCA | T98A | NP_055782.3 |
XM_005254232.4 | 587 | Missense Mutation | ACA,GCA | T98A | XP_005254289.1 |
XM_005254234.4 | 587 | Missense Mutation | ACA,GCA | T98A | XP_005254291.1 |
XM_005254235.3 | 587 | Missense Mutation | ACA,GCA | T98A | XP_005254292.1 |
XM_011521370.2 | 587 | Intron | XP_011519672.1 | ||
XM_011521371.1 | 587 | UTR 5 | XP_011519673.1 | ||
XM_011521372.2 | 587 | Missense Mutation | ACA,GCA | T98A | XP_011519674.1 |
XM_017022012.1 | 587 | UTR 5 | XP_016877501.1 | ||
XM_017022013.1 | 587 | UTR 5 | XP_016877502.1 |