Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199096.1 | 702 | Intron | NP_001186025.1 | ||
NM_001199097.1 | 702 | Intron | NP_001186026.1 | ||
NM_001199098.1 | 702 | Intron | NP_001186027.1 | ||
NM_001199099.1 | 702 | Intron | NP_001186028.1 | ||
NM_001286464.1 | 702 | Intron | NP_001273393.1 | ||
NM_003933.4 | 702 | Missense Mutation | CAC,TAC | H17Y | NP_003924.2 |
XM_011522728.1 | 702 | Missense Mutation | CAC,TAC | H17Y | XP_011521030.1 |
XM_011522729.1 | 702 | Missense Mutation | CAC,TAC | H17Y | XP_011521031.1 |
XM_011522730.2 | 702 | Missense Mutation | CAC,TAC | H17Y | XP_011521032.1 |