Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001276479.1 | 2677 | Missense Mutation | ACC,GCC | T882A | NP_001263408.1 |
NM_001276480.1 | 2677 | Missense Mutation | ACC,GCC | T750A | NP_001263409.1 |
NM_004793.3 | 2677 | Missense Mutation | ACC,GCC | T946A | NP_004784.2 |
XM_011528441.2 | 2677 | Intron | XP_011526743.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015414.3 | 2677 | Intron | NP_056229.2 | ||
NM_033643.2 | 2677 | Intron | NP_378669.1 |