Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297755.1 | 228 | Intron | NP_001284684.1 | ||
NM_001297756.1 | 228 | Intron | NP_001284685.1 | ||
NM_001297757.1 | 228 | Intron | NP_001284686.1 | ||
NM_001297758.1 | 228 | Intron | NP_001284687.1 | ||
NM_001297759.1 | 228 | Intron | NP_001284688.1 | ||
NM_133636.3 | 228 | Intron | NP_598375.2 | ||
XM_005262711.1 | 228 | Intron | XP_005262768.1 | ||
XM_005262713.2 | 228 | Intron | XP_005262770.1 | ||
XM_006714076.2 | 228 | Intron | XP_006714139.1 | ||
XM_011531580.2 | 228 | Intron | XP_011529882.1 | ||
XM_017007679.1 | 228 | Intron | XP_016863168.1 | ||
XM_017007680.1 | 228 | Intron | XP_016863169.1 | ||
XM_017007681.1 | 228 | Intron | XP_016863170.1 | ||
XM_017007682.1 | 228 | Intron | XP_016863171.1 | ||
XM_017007683.1 | 228 | Intron | XP_016863172.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297767.1 | 228 | Missense Mutation | CAT,TAT | H28Y | NP_001284696.1 |
NM_001297769.1 | 228 | Missense Mutation | CAT,TAT | H28Y | NP_001284698.1 |
NM_001297770.1 | 228 | Missense Mutation | CAT,TAT | H28Y | NP_001284699.1 |
NM_016067.3 | 228 | Missense Mutation | CAT,TAT | H28Y | NP_057151.1 |