Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001005862.2 | 3916 | Missense Mutation | CAT,GAT | H1114D | NP_001005862.1 |
NM_001289936.1 | 3916 | Missense Mutation | CAT,GAT | H1129D | NP_001276865.1 |
NM_001289937.1 | 3916 | UTR 3 | NP_001276866.1 | ||
NM_001289938.1 | 3916 | Intron | NP_001276867.1 | ||
NM_004448.3 | 3916 | Missense Mutation | CAT,GAT | H1144D | NP_004439.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_032339.4 | 3916 | Intron | NP_115715.3 | ||
XM_005257736.3 | 3916 | Intron | XP_005257793.1 |