Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001318204.1 | 1538 | Intron | NP_001305133.1 | ||
NM_004560.3 | 1538 | Missense Mutation | CAC,CCC | H878P | NP_004551.2 |
XM_005252008.4 | 1538 | Missense Mutation | CAC,CCC | H738P | XP_005252065.1 |
XM_005252009.3 | 1538 | Missense Mutation | CAC,CCC | H477P | XP_005252066.1 |
XM_006717121.3 | 1538 | Missense Mutation | CAC,CCC | H738P | XP_006717184.1 |
XM_017014762.1 | 1538 | Missense Mutation | CAC,CCC | H875P | XP_016870251.1 |
XM_017014763.1 | 1538 | Missense Mutation | CAC,CCC | H738P | XP_016870252.1 |