Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001012502.2 | 329 | Missense Mutation | CAT,GAT | H96D | NP_001012520.2 |
XM_006717064.3 | 329 | Missense Mutation | CAT,GAT | H191D | XP_006717127.2 |
XM_011518559.2 | 329 | Missense Mutation | CAT,GAT | H191D | XP_011516861.2 |
XM_017014629.1 | 329 | Missense Mutation | CAT,GAT | H191D | XP_016870118.1 |
XM_017014630.1 | 329 | UTR 5 | XP_016870119.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001002913.1 | 329 | Intron | NP_001002913.1 | ||
XM_006716955.3 | 329 | Intron | XP_006717018.1 | ||
XM_017014276.1 | 329 | Intron | XP_016869765.1 | ||
XM_017014277.1 | 329 | Intron | XP_016869766.1 | ||
XM_017014278.1 | 329 | Intron | XP_016869767.1 |