Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135105.1 | 844 | Missense Mutation | CCC,CGC | P277R | NP_001128577.1 |
NM_001135106.1 | 844 | Intron | NP_001128578.1 | ||
NM_001135107.1 | 844 | Intron | NP_001128579.1 | ||
NM_032115.3 | 844 | Intron | NP_115491.1 | ||
XM_011514935.2 | 844 | Intron | XP_011513237.1 | ||
XM_017011346.1 | 844 | Intron | XP_016866835.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135111.1 | 844 | Intron | NP_001128583.1 | ||
NM_031460.3 | 844 | Intron | NP_113648.2 |