Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256826.1 | 1630 | Silent Mutation | CCA,CCG | P433P | NP_001243755.1 |
NM_019088.3 | 1630 | Missense Mutation | AGT,GGT | S505G | NP_061961.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303614.1 | 1630 | Intron | NP_001290543.1 | ||
NM_018028.3 | 1630 | Intron | NP_060498.2 | ||
XM_011527057.2 | 1630 | Intron | XP_011525359.1 | ||
XM_011527060.2 | 1630 | Intron | XP_011525362.1 | ||
XM_011527061.2 | 1630 | Intron | XP_011525363.1 | ||
XM_011527062.2 | 1630 | Intron | XP_011525364.1 | ||
XM_011527063.2 | 1630 | Intron | XP_011525365.1 | ||
XM_011527064.2 | 1630 | Intron | XP_011525366.1 | ||
XM_017026918.1 | 1630 | Intron | XP_016882407.1 | ||
XM_017026919.1 | 1630 | Intron | XP_016882408.1 | ||
XM_017026920.1 | 1630 | Intron | XP_016882409.1 | ||
XM_017026921.1 | 1630 | Intron | XP_016882410.1 | ||
XM_017026922.1 | 1630 | Intron | XP_016882411.1 | ||
XM_017026923.1 | 1630 | Intron | XP_016882412.1 |