ENST00000506007.2:n.1908G=
|
|
|
ENST00000513232.2:c.*333G=
|
ENSP00000422749.2:n.*333G=
|
|
ENST00000698450.1:n.1002G=
|
|
|
ENST00000698451.1:n.1038G=
|
|
|
ENST00000698452.1:n.2109G=
|
|
|
ENST00000698453.1:c.1618G=
|
ENSP00000513735.1:p.Glu540=
|
|
ENST00000698454.1:c.1609G=
|
ENSP00000513736.1:p.Glu537=
|
|
ENST00000698455.1:c.*1594G=
|
ENSP00000513737.1:n.*1594G=
|
|
ENST00000698456.1:c.*476G=
|
ENSP00000513738.1:n.*476G=
|
|
ENST00000698457.1:c.1618G=
|
ENSP00000513739.1:p.Glu540=
|
|
ENST00000698458.1:c.1654G=
|
ENSP00000513740.1:p.Glu552=
|
|
ENST00000698459.1:c.1618G=
|
ENSP00000513741.1:p.Glu540=
|
|
ENST00000698460.1:c.1618G=
|
ENSP00000513742.1:p.Glu540=
|
|
ENST00000698461.1:n.1908G=
|
|
|
ENST00000698462.1:n.1908G=
|
|
|
ENST00000698468.1:n.2109G=
|
|
|
ENST00000698469.1:c.*965G=
|
ENSP00000513743.1:n.*965G=
|
|
ENST00000698470.1:c.1618G=
|
ENSP00000513744.1:p.Glu540=
|
|
ENST00000698471.1:n.1908G=
|
|
|
ENST00000698472.1:c.*333G=
|
ENSP00000513745.1:n.*333G=
|
|
ENST00000698473.1:n.1908G=
|
|
|
ENST00000698474.1:n.1908G=
|
|
|
ENST00000698475.1:n.1908G=
|
|
|
ENST00000698476.1:c.1618G=
|
ENSP00000513746.1:p.Glu540=
|
|
ENST00000698477.1:c.1618G=
|
ENSP00000513747.1:p.Glu540=
|
|
ENST00000698478.1:n.1908G=
|
|
|
ENST00000698479.1:c.1618G=
|
ENSP00000513748.1:p.Glu540=
|
|
ENST00000698480.1:c.1618G=
|
ENSP00000513749.1:p.Glu540=
|
|
ENST00000698481.1:c.1618G=
|
ENSP00000513750.1:p.Glu540=
|
|
ENST00000698482.1:n.1908G=
|
|
|
ENST00000698483.1:n.1908G=
|
|
|
ENST00000698484.1:c.1618G=
|
ENSP00000513751.1:p.Glu540=
|
|
ENST00000698485.1:c.1618G=
|
ENSP00000513752.1:p.Glu540=
|
|
ENST00000698486.1:n.1908G=
|
|
|
ENST00000698487.1:c.1618G=
|
ENSP00000513753.1:p.Glu540=
|
|
ENST00000698488.1:c.1618G=
|
ENSP00000513754.1:p.Glu540=
|
|
ENST00000698489.1:n.5693G=
|
|
|
ENST00000698490.1:c.1618G=
|
ENSP00000513755.1:p.Glu540=
|
|
ENST00000698492.1:c.*333G=
|
ENSP00000513756.1:n.*333G=
|
|
ENST00000698493.1:n.1908G=
|
|
|
ENST00000698494.1:c.1618G=
|
ENSP00000513757.1:p.Glu540=
|
|
ENST00000358746.7:c.1618G=
MANE Select
|
ENSP00000351596.3:p.Glu540=
|
|
ENST00000649566.1:c.1618G=
|
ENSP00000497948.1:p.Glu540=
|
|
ENST00000358746.6:c.1618G=
|
ENSP00000351596.2:p.Glu540=
|
|
ENST00000505578.5:c.320-343G=
|
ENSP00000423141.1:n.320-343G=
|
|
ENST00000513232.1:c.435G=
|
ENSP00000422749.1:n.435G=
|
|
ENST00000514952.5:c.1474G=
|
ENSP00000423742.1:p.Glu492=
|
|
NM_014639.3:c.1618G= , LRG_173t1:c.1618G=
|
NP_055454.1:p.Glu540=
|
|
XR_948312.1:n.1887G=
|
|
|
XR_001742370.2:n.1890G=
|
|
|
NM_014639.4:c.1618G=
MANE Select
|
NP_055454.1:p.Glu540=
|
|