|
ENST00000361166.10:c.913G=
|
ENSP00000354529.6:p.Glu305=
|
|
|
ENST00000673312.2:c.*542G=
|
ENSP00000500186.2:n.*542G=
|
|
|
ENST00000338641.10:c.1048G=
MANE Select
|
ENSP00000344666.5:p.Glu350=
|
|
|
ENST00000361166.9:c.466G=
|
ENSP00000354529.5:p.Glu156=
|
|
|
ENST00000672461.1:c.1048G=
|
ENSP00000500919.1:p.Glu350=
|
|
|
ENST00000672805.1:c.*930G=
|
ENSP00000500295.1:n.*930G=
|
|
|
ENST00000672896.1:c.1048G=
|
ENSP00000500117.1:p.Glu350=
|
|
|
ENST00000673312.1:c.1067G=
|
ENSP00000500186.1:n.1067G=
|
|
|
ENST00000334961.11:c.799G=
|
ENSP00000335652.7:p.Glu267=
|
|
|
ENST00000338641.8:c.1048G=
|
ENSP00000344666.4:p.Glu350=
|
|
|
ENST00000353887.8:c.799G=
|
ENSP00000340626.4:p.Glu267=
|
|
|
ENST00000361166.8:c.1048G=
|
ENSP00000354529.4:p.Glu350=
|
|
|
ENST00000361452.8:c.925G=
|
ENSP00000354897.4:p.Glu309=
|
|
|
ENST00000361676.8:c.922G=
|
ENSP00000355183.4:p.Glu308=
|
|
|
ENST00000397789.3:c.1048G=
|
ENSP00000380891.3:p.Glu350=
|
|
|
ENST00000403435.5:c.1000-39G=
|
ENSP00000384029.1:n.1000-39G=
|
|
|
ENST00000403999.7:c.1048G=
|
ENSP00000384797.3:p.Glu350=
|
|
|
ENST00000413209.6:c.448-22878G=
|
ENSP00000409921.2:n.448-22878G=
|
|
|
ENST00000432151.5:c.523-2962G=
|
ENSP00000395885.1:n.523-2962G=
|
|
|
NM_000268.3:c.1048G= , LRG_511t1:c.1048G=
|
NP_000259.1:p.Glu350=
|
|
|
NM_016418.5:c.1048G= , LRG_511t2:c.1048G=
|
NP_057502.2:p.Glu350=
|
|
|
NM_181825.2:c.1048G=
|
NP_861546.1:p.Glu350=
|
|
|
NM_181828.2:c.922G=
|
NP_861966.1:p.Glu308=
|
|
|
NM_181829.2:c.925G=
|
NP_861967.1:p.Glu309=
|
|
|
NM_181830.2:c.799G=
|
NP_861968.1:p.Glu267=
|
|
|
NM_181831.2:c.799G=
|
NP_861969.1:p.Glu267=
|
|
|
NM_181832.2:c.1048G=
|
NP_861970.1:p.Glu350=
|
|
|
NM_181833.2:c.448-22878G=
|
NP_861971.1:n.448-22878G=
|
|
|
NR_156186.1:n.1607G=
|
|
|
|
XM_017028809.2:c.934G=
|
XP_016884298.1:p.Glu312=
|
|
|
XM_017028810.1:c.934G=
|
XP_016884299.1:p.Glu312=
|
|
|
NM_000268.4:c.1048G=
MANE Select
|
NP_000259.1:p.Glu350=
|
|
|
NM_181825.3:c.1048G=
|
NP_861546.1:p.Glu350=
|
|
|
NM_181828.3:c.922G=
|
NP_861966.1:p.Glu308=
|
|
|
NM_181829.3:c.925G=
|
NP_861967.1:p.Glu309=
|
|
|
NM_181830.3:c.799G=
|
NP_861968.1:p.Glu267=
|
|
|
NM_181831.3:c.799G=
|
NP_861969.1:p.Glu267=
|
|
|
NM_181832.3:c.1048G=
|
NP_861970.1:p.Glu350=
|
|
|
NR_156186.2:n.1530G=
|
|
|
|
NM_181833.3:c.448-22878G=
|
NP_861971.1:n.448-22878G=
|
|
