Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004314.2 | 4428 | Intron | NP_004305.2 | ||
XM_011520114.2 | 4428 | Intron | XP_011518416.1 | ||
XM_017017763.1 | 4428 | Intron | XP_016873252.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303034.1 | 4428 | Missense Mutation | CAA,CGA | Q181R | NP_001289963.1 |
NM_001303035.1 | 4428 | Missense Mutation | CAA,CGA | Q181R | NP_001289964.1 |
NM_020402.3 | 4428 | Missense Mutation | CAA,CGA | Q387R | NP_065135.2 |
XM_011520234.1 | 4428 | Missense Mutation | CAA,CGA | Q181R | XP_011518536.1 |