Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001320412.1 | 2760 | UTR 3 | NP_001307341.1 | ||
NM_006657.2 | 2760 | UTR 3 | NP_006648.1 | ||
NM_206965.1 | 2760 | Intron | NP_996848.1 | ||
XM_006723961.3 | 2760 | Intron | XP_006724024.2 | ||
XM_006723962.3 | 2760 | Intron | XP_006724025.2 | ||
XM_011529434.2 | 2760 | Missense Mutation | CCG,CTG | P641L | XP_011527736.1 |
XM_011529435.2 | 2760 | Missense Mutation | CCG,CTG | P598L | XP_011527737.1 |
XM_011529436.2 | 2760 | UTR 3 | XP_011527738.1 | ||
XM_011529437.2 | 2760 | UTR 3 | XP_011527739.1 | ||
XM_011529439.2 | 2760 | Missense Mutation | CCG,CTG | P470L | XP_011527741.1 |
XM_011529440.2 | 2760 | Intron | XP_011527742.1 |