Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001324191.1 | 298 | UTR 5 | NP_001311120.1 | ||
NM_001324192.1 | 298 | Missense Mutation | CGT,CTT | R44L | NP_001311121.1 |
NM_001324193.1 | 298 | Intron | NP_001311122.1 | ||
NM_024960.5 | 298 | Intron | NP_079236.3 | ||
NM_153638.3 | 298 | Missense Mutation | CGT,CTT | R44L | NP_705902.2 |
NM_153640.3 | 298 | Intron | NP_705904.1 | ||
XM_005260835.3 | 298 | Intron | XP_005260892.1 | ||
XM_005260836.4 | 298 | Intron | XP_005260893.3 | ||
XM_011529364.2 | 298 | Missense Mutation | CGT,CTT | R44L | XP_011527666.1 |
XM_011529365.2 | 298 | Missense Mutation | CGT,CTT | R44L | XP_011527667.1 |
XM_017028077.1 | 298 | Intron | XP_016883566.1 | ||
XM_017028078.1 | 298 | Intron | XP_016883567.1 | ||
XM_017028079.1 | 298 | Intron | XP_016883568.1 |