Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018842.4 | 2655 | UTR 3 | NP_061330.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001159491.1 | 2655 | Missense Mutation | ACG,ATG | T91M | NP_001152963.1 |
NM_015379.4 | 2655 | Intron | NP_056194.1 | ||
XM_017011931.1 | 2655 | Intron | XP_016867420.1 | ||
XM_017011932.1 | 2655 | Intron | XP_016867421.1 | ||
XM_017011933.1 | 2655 | Intron | XP_016867422.1 | ||
XM_017011934.1 | 2655 | Intron | XP_016867423.1 | ||
XM_017011935.1 | 2655 | Intron | XP_016867424.1 | ||
XM_017011936.1 | 2655 | Intron | XP_016867425.1 |