|
ENST00000287152.12:c.2149C>G
MANE Select
|
ENSP00000287152.7:p.His717Asp
|
|
|
ENST00000229913.9:c.502C>G
|
ENSP00000229913.5:p.His168Asp
|
|
|
ENST00000287152.11:c.2149C>G
|
ENSP00000287152.7:p.His717Asp
|
|
|
ENST00000394362.5:c.502C>G
|
ENSP00000377889.1:p.His168Asp
|
|
|
ENST00000458470.5:c.1824C>G
|
|
|
|
ENST00000538893.5:c.502C>G
|
ENSP00000441435.2:p.His168Asp
|
|
|
NM_001289020.1:c.2098C>G
|
NP_001275949.1:p.His700Asp
|
|
|
NM_001289021.1:c.1981C>G
|
NP_001275950.1:p.His661Asp
|
|
|
NM_001289024.1:c.502C>G
|
NP_001275953.1:p.His168Asp
|
|
|
NM_145027.4:c.2149C>G
|
NP_659464.3:p.His717Asp
|
|
|
XM_005248904.3:c.2149C>G
|
XP_005248961.1:p.His717Asp
|
|
|
XM_011514357.1:c.2149C>G
|
XP_011512659.1:p.His717Asp
|
|
|
XM_011514358.1:c.2149C>G
|
XP_011512660.1:p.His717Asp
|
|
|
XM_011514359.1:c.2149C>G
|
XP_011512661.1:p.His717Asp
|
|
|
XM_011514360.1:c.1522C>G
|
XP_011512662.1:p.His508Asp
|
|
|
NM_001289020.2:c.2098C>G
|
NP_001275949.1:p.His700Asp
|
|
|
NM_001289021.2:c.1981C>G
|
NP_001275950.1:p.His661Asp
|
|
|
NM_001289024.2:c.502C>G
|
NP_001275953.1:p.His168Asp
|
|
|
NM_001351566.1:c.502C>G
|
NP_001338495.1:p.His168Asp
|
|
|
NM_145027.5:c.2149C>G
|
NP_659464.3:p.His717Asp
|
|
|
XM_005248904.4:c.2149C>G
|
XP_005248961.1:p.His717Asp
|
|
|
XM_011514357.3:c.2149C>G
|
XP_011512659.1:p.His717Asp
|
|
|
XM_011514358.3:c.2149C>G
|
XP_011512660.1:p.His717Asp
|
|
|
XM_011514359.3:c.2149C>G
|
XP_011512661.1:p.His717Asp
|
|
|
XM_017010427.1:c.1840C>G
|
XP_016865916.1:p.His614Asp
|
|
|
XM_017010428.1:c.1504C>G
|
XP_016865917.1:p.His502Asp
|
|
|
XR_001744111.1:n.75+5360G>C
|
|
|
|
NM_145027.6:c.2149C>G
MANE Select
|
NP_659464.3:p.His717Asp
|
|
|
NM_001289020.3:c.2098C>G
|
NP_001275949.1:p.His700Asp
|
|
|
NM_001289021.3:c.1981C>G
|
NP_001275950.1:p.His661Asp
|
|
|
NM_001289024.3:c.502C>G
|
NP_001275953.1:p.His168Asp
|
|
|
NM_001351566.2:c.502C>G
|
NP_001338495.1:p.His168Asp
|
|
