Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001170961.1 | 3402 | Missense Mutation | CAT,CGT | H1040R | NP_001164432.1 |
NM_001170962.1 | 3402 | Missense Mutation | CAT,CGT | H1026R | NP_001164433.1 |
NM_001170963.1 | 3402 | Intron | NP_001164434.1 | ||
NM_001555.4 | 3402 | Missense Mutation | CAT,CGT | H1035R | NP_001546.2 |
NM_205833.3 | 3402 | Intron | NP_991402.1 | ||
XM_011531330.1 | 3402 | Missense Mutation | CAT,CGT | H1040R | XP_011529632.1 |
XM_011531333.1 | 3402 | Missense Mutation | CAT,CGT | H1040R | XP_011529635.1 |
XM_011531334.1 | 3402 | Intron | XP_011529636.1 |