Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321086.1 | 531 | Intron | NP_001308015.1 | ||
NM_002517.3 | 531 | Intron | NP_002508.2 | ||
XM_006723231.2 | 531 | Intron | XP_006723294.1 | ||
XM_011526997.1 | 531 | Intron | XP_011525299.1 | ||
XM_011526999.1 | 531 | Intron | XP_011525301.1 | ||
XM_011527001.1 | 531 | Intron | XP_011525303.1 | ||
XM_011527002.1 | 531 | Intron | XP_011525304.1 | ||
XM_011527006.1 | 531 | Intron | XP_011525308.1 | ||
XM_011527007.1 | 531 | Intron | XP_011525309.1 | ||
XM_017026841.1 | 531 | Intron | XP_016882330.1 | ||
XM_017026842.1 | 531 | Intron | XP_016882331.1 | ||
XM_017026843.1 | 531 | Intron | XP_016882332.1 | ||
XM_017026844.1 | 531 | Intron | XP_016882333.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_017854.1 | 531 | Missense Mutation | CGC,TGC | R76C | NP_060324.1 |
XM_017026917.1 | 531 | UTR 5 | XP_016882406.1 |