Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008228.2 | 709 | Intron | NP_001008229.1 | ||
NM_001008229.2 | 709 | Intron | NP_001008230.1 | ||
NM_001170418.1 | 709 | Intron | NP_001163889.1 | ||
NM_002433.4 | 709 | Intron | NP_002424.3 | ||
NM_206809.3 | 709 | Intron | NP_996532.2 | ||
NM_206810.3 | 709 | Intron | NP_996533.2 | ||
NM_206811.3 | 709 | Intron | NP_996534.2 | ||
NM_206812.3 | 709 | Intron | NP_996535.2 | ||
NM_206814.5 | 709 | Intron | NP_996537.3 | ||
XM_005249131.3 | 709 | Intron | XP_005249188.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001109809.2 | 709 | Missense Mutation | CAT,CGT | H248R | NP_001103279.2 |
XM_006715087.3 | 709 | Missense Mutation | CAT,CGT | H176R | XP_006715150.1 |
XM_011514570.2 | 709 | Missense Mutation | CAT,CGT | H248R | XP_011512872.1 |