Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001227.4 | 142 | UTR 5 | NP_001218.1 | ||
NM_001267056.1 | 142 | Intron | NP_001253985.1 | ||
NM_001267057.1 | 142 | Missense Mutation | ACC,ATC | T19I | NP_001253986.1 |
NM_001267058.1 | 142 | Intron | NP_001253987.1 | ||
NM_001320911.1 | 142 | Intron | NP_001307840.1 | ||
NM_033338.5 | 142 | UTR 5 | NP_203124.1 | ||
NM_033339.4 | 142 | UTR 5 | NP_203125.1 | ||
NM_033340.3 | 142 | Intron | NP_203126.1 | ||
XM_006718017.3 | 142 | Intron | XP_006718080.1 | ||
XM_011540260.1 | 142 | Intron | XP_011538562.1 | ||
XM_017016763.1 | 142 | Intron | XP_016872252.1 | ||
XM_017016764.1 | 142 | Intron | XP_016872253.1 |