Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012435.2 | 1582 | Missense Mutation | ACC,GCC | T568A | NP_036567.2 |
XM_011527893.2 | 1582 | Intron | XP_011526195.1 | ||
XM_011527894.2 | 1582 | Intron | XP_011526196.1 | ||
XM_011527895.2 | 1582 | Missense Mutation | ACC,GCC | T523A | XP_011526197.1 |
XM_011527896.2 | 1582 | Intron | XP_011526198.1 | ||
XM_017026567.1 | 1582 | Intron | XP_016882056.1 |