Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001171191.1 | 419 | Missense Mutation | CAT,CGT | H102R | NP_001164662.1 |
NM_001171192.1 | 419 | Missense Mutation | CAT,CGT | H181R | NP_001164663.1 |
NM_001171193.1 | 419 | Missense Mutation | CAT,CGT | H102R | NP_001164664.1 |
NM_017711.3 | 419 | Missense Mutation | CAT,CGT | H181R | NP_060181.2 |
XM_011530977.1 | 419 | Missense Mutation | CAT,CGT | H54R | XP_011529279.1 |
XM_017029614.1 | 419 | UTR 5 | XP_016885103.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_011531081.2 | 419 | Intron | XP_011529383.1 | ||
XM_011531082.2 | 419 | Intron | XP_011529384.1 |