Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001135746.1 | 710 | Missense Mutation | CAT,CGT | H12R | NP_001129218.1 |
NM_001135747.1 | 710 | Intron | NP_001129219.1 | ||
NM_001135748.1 | 710 | Missense Mutation | CAT,CGT | H12R | NP_001129220.1 |
NM_145043.2 | 710 | Missense Mutation | CAT,CGT | H12R | NP_659480.1 |
XM_005272382.2 | 710 | UTR 5 | XP_005272439.1 | ||
XM_005272383.2 | 710 | Intron | XP_005272440.1 | ||
XM_017013301.1 | 710 | UTR 5 | XP_016868790.1 |