Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_134268.4 | 474 | Missense Mutation | CAT,CGT | H155R | NP_599030.1 |
XM_005257005.2 | 474 | Missense Mutation | CAT,CGT | H155R | XP_005257062.1 |
XM_017024116.1 | 474 | Missense Mutation | CAT,CGT | H90R | XP_016879605.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001077620.2 | 474 | Intron | NP_001071088.1 | ||
XM_017025013.1 | 474 | Intron | XP_016880502.1 | ||
XM_017025014.1 | 474 | Intron | XP_016880503.1 | ||
XM_017025015.1 | 474 | Intron | XP_016880504.1 |