Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004542.3 | 479 | Missense Mutation | GCC,GGC | A12G | NP_004533.1 |
XM_017026833.1 | 479 | Missense Mutation | GCC,GGC | A12G | XP_016882322.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001282349.1 | 479 | Intron | NP_001269278.1 | ||
NM_001282350.1 | 479 | Intron | NP_001269279.1 | ||
NM_130771.4 | 479 | Intron | NP_570127.3 | ||
NM_133168.4 | 479 | Intron | NP_573398.2 | ||
NM_133169.4 | 479 | Intron | NP_573399.2 | ||
NM_206818.2 | 479 | Intron | NP_996554.2 |