Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003782.3 | 947 | Missense Mutation | CCT,TCT | P223S | NP_003773.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164267.1 | 947 | Intron | NP_001157739.1 | ||
NM_005452.5 | 947 | Intron | NP_005443.3 | ||
XM_017011484.1 | 947 | Intron | XP_016866973.1 | ||
XM_017011485.1 | 947 | Intron | XP_016866974.1 | ||
XM_017011486.1 | 947 | Intron | XP_016866975.1 | ||
XM_017011487.1 | 947 | Intron | XP_016866976.1 |