Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145815.1 | 1877 | Missense Mutation | CCC,GCC | P594A | NP_001139287.1 |
NM_015944.3 | 1877 | Intron | NP_057028.2 | ||
XM_017023262.1 | 1877 | UTR 3 | XP_016878751.1 | ||
XM_017023263.1 | 1877 | UTR 3 | XP_016878752.1 | ||
XM_017023264.1 | 1877 | UTR 3 | XP_016878753.1 | ||
XM_017023265.1 | 1877 | UTR 3 | XP_016878754.1 | ||
XM_017023266.1 | 1877 | UTR 3 | XP_016878755.1 | ||
XM_017023267.1 | 1877 | UTR 3 | XP_016878756.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001048212.3 | 1877 | Missense Mutation | GCG,GGG | A107G | NP_001041677.1 |