Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001128631.2 | 1047 | Missense Mutation | ACC,GCC | T231A | NP_001122103.1 |
NM_001288654.2 | 1047 | Missense Mutation | ACC,GCC | T231A | NP_001275583.1 |
NM_001288655.1 | 1047 | Missense Mutation | ACC,GCC | T231A | NP_001275584.1 |
NM_001321326.1 | 1047 | Missense Mutation | ACC,GCC | T231A | NP_001308255.1 |
NM_024819.6 | 1047 | Missense Mutation | ACC,GCC | T231A | NP_079095.3 |
XM_005257688.2 | 1047 | Intron | XP_005257745.1 | ||
XM_011525262.2 | 1047 | Missense Mutation | ACC,GCC | T231A | XP_011523564.1 |
XM_017025102.1 | 1047 | Intron | XP_016880591.1 | ||
XM_017025103.1 | 1047 | Intron | XP_016880592.1 | ||
XM_017025104.1 | 1047 | Intron | XP_016880593.1 | ||
XM_017025105.1 | 1047 | Missense Mutation | ACC,GCC | T130A | XP_016880594.1 |
XM_017025106.1 | 1047 | Missense Mutation | ACC,GCC | T130A | XP_016880595.1 |