|
ENST00000243189.12:c.716A>C
MANE Select
|
ENSP00000243189.7:p.Glu239Ala
|
|
|
ENST00000243189.11:c.716A>C
|
ENSP00000243189.7:p.Glu239Ala
|
|
|
ENST00000473314.6:c.*671A>C
|
ENSP00000457582.1:n.*671A>C
|
|
|
ENST00000475766.2:n.267A>C
|
|
|
|
ENST00000498238.1:n.2444A>C
|
|
|
|
ENST00000564223.5:n.65A>C
|
|
|
|
ENST00000565733.5:c.393A>C
|
|
|
|
ENST00000566395.5:c.333A>C
|
|
|
|
ENST00000568254.5:c.*626A>C
|
ENSP00000457195.1:n.*626A>C
|
|
|
ENST00000569495.5:n.516A>C
|
|
|
|
ENST00000570063.5:n.1353A>C
|
|
|
|
NM_020317.3:c.716A>C
|
NP_064713.3:p.Glu239Ala
|
|
|
XM_011541797.1:c.716A>C
|
XP_011540099.1:p.Glu239Ala
|
|
|
XM_011541798.1:c.*79A>C
|
XP_011540100.1:n.*79A>C
|
|
|
XR_241200.1:n.1629A>C
|
|
|
|
XR_241201.1:n.1038A>C
|
|
|
|
XR_946709.1:n.2280A>C
|
|
|
|
XR_946710.1:n.1962A>C
|
|
|
|
XR_946711.1:n.1689A>C
|
|
|
|
XR_946712.1:n.1858A>C
|
|
|
|
XR_946713.1:n.1584A>C
|
|
|
|
NM_001321772.1:c.716A>C
|
NP_001308701.1:p.Glu239Ala
|
|
|
NM_020317.4:c.716A>C
|
NP_064713.3:p.Glu239Ala
|
|
|
NR_135143.1:n.2509A>C
|
|
|
|
NR_135144.1:n.1584A>C
|
|
|
|
NR_135777.1:n.2484A>C
|
|
|
|
NR_135778.1:n.1858A>C
|
|
|
|
NR_135780.1:n.1962A>C
|
|
|
|
NR_135781.1:n.1629A>C
|
|
|
|
NR_135782.1:n.1311A>C
|
|
|
|
NR_135783.1:n.1038A>C
|
|
|
|
NR_135784.1:n.2509A>C
|
|
|
|
NR_135785.1:n.1037A>C
|
|
|
|
NR_135786.1:n.2509A>C
|
|
|
|
NR_135787.1:n.2633A>C
|
|
|
|
NR_135788.1:n.2575A>C
|
|
|
|
NR_135789.1:n.3513A>C
|
|
|
|
XR_946709.2:n.2246A>C
|
|
|
|
NM_020317.5:c.716A>C
MANE Select
|
NP_064713.3:p.Glu239Ala
|
|
|
NR_135784.2:n.2444A>C
|
|
|
|
NR_135786.2:n.2444A>C
|
|
|
|
NM_001321772.2:c.716A>C
|
NP_001308701.1:p.Glu239Ala
|
|
|
NR_135143.2:n.2444A>C
|
|
|
|
NR_135144.2:n.1519A>C
|
|
|
|
NR_135777.2:n.2484A>C
|
|
|
|
NR_135778.2:n.1793A>C
|
|
|
|
NR_135780.2:n.1897A>C
|
|
|
|
NR_135781.2:n.1564A>C
|
|
|
|
NR_135782.2:n.1246A>C
|
|
|
|
NR_135783.2:n.973A>C
|
|
|
|
NR_135785.2:n.972A>C
|
|
|
|
NR_135787.2:n.2633A>C
|
|
|
|
NR_135788.2:n.2575A>C
|
|
|
|
NR_135789.2:n.3513A>C
|
|
|
