ENST00000683044.1:c.*1113A>G
|
ENSP00000507095.1:n.*1113A>G
|
|
ENST00000683288.1:c.*2041A>G
|
ENSP00000507477.1:n.*2041A>G
|
|
ENST00000683748.1:c.2069A>G
|
ENSP00000507377.1:p.His690Arg
|
|
ENST00000683905.1:c.*718A>G
|
ENSP00000506960.1:n.*718A>G
|
|
ENST00000684139.1:c.1577A>G
|
ENSP00000507295.1:p.His526Arg
|
|
ENST00000684210.1:n.1755A>G
|
|
|
ENST00000684314.1:c.1937A>G
|
ENSP00000507700.1:p.His646Arg
|
|
ENST00000684331.1:c.*762A>G
|
ENSP00000507431.1:n.*762A>G
|
|
ENST00000684463.1:n.680A>G
|
|
|
ENST00000684646.1:c.1829A>G
|
ENSP00000507723.1:p.His610Arg
|
|
ENST00000309971.9:c.2042A>G
MANE Select
|
ENSP00000308622.5:p.His681Arg
|
|
ENST00000309971.8:c.2042A>G
|
ENSP00000308622.4:p.His681Arg
|
|
NM_001003722.1:c.2042A>G , LRG_484t1:c.2042A>G
|
NP_001003722.1:p.His681Arg
|
|
XM_006717059.2:c.2078A>G
|
XP_006717122.1:p.His693Arg
|
|
XM_006717060.2:c.2051A>G
|
XP_006717123.1:p.His684Arg
|
|
XM_011518549.1:c.2078A>G
|
XP_011516851.1:p.His693Arg
|
|
XM_011518550.1:c.2078A>G
|
XP_011516852.1:p.His693Arg
|
|
XM_011518551.1:c.2069A>G
|
XP_011516853.1:p.His690Arg
|
|
XM_011518552.1:c.1319A>G
|
XP_011516854.1:p.His440Arg
|
|
XR_242681.3:n.100+2264T>C
|
|
|
XM_006717059.3:c.2078A>G
|
XP_006717122.1:p.His693Arg
|
|
XM_006717060.3:c.2051A>G
|
XP_006717123.1:p.His684Arg
|
|
XM_011518551.2:c.2069A>G
|
XP_011516853.1:p.His690Arg
|
|
XM_024447519.1:c.2051A>G
|
XP_024303287.1:p.His684Arg
|
|
NM_001003722.2:c.2042A>G
MANE Select
|
NP_001003722.1:p.His681Arg
|
|