|
ENST00000413740.2:c.1668-1494A>T
|
ENSP00000416476.2:n.1668-1494A>T
|
|
|
ENST00000429117.6:c.1784A>T
|
ENSP00000407019.2:p.Glu595Val
|
|
|
ENST00000450420.6:c.1559-1494A>T
|
ENSP00000393006.2:n.1559-1494A>T
|
|
|
ENST00000456676.7:c.1896+1309A>T
|
ENSP00000416687.3:n.1896+1309A>T
|
|
|
ENST00000492474.6:c.1355A>T
|
ENSP00000518393.1:p.Glu452Val
|
|
|
ENST00000616768.6:c.1985A>T
|
ENSP00000480669.3:p.Glu662Val
|
|
|
ENST00000673673.2:c.1913A>T
|
ENSP00000500979.2:p.Glu638Val
|
|
|
ENST00000231790.8:c.2078A>T
MANE Select
|
ENSP00000231790.3:p.Glu693Val
|
|
|
ENST00000413212.2:c.*996A>T
|
ENSP00000400844.2:n.*996A>T
|
|
|
ENST00000432299.6:c.*1910A>T
|
ENSP00000416783.1:n.*1910A>T
|
|
|
ENST00000447829.6:c.*1189A>T
|
ENSP00000399329.2:n.*1189A>T
|
|
|
ENST00000539477.6:c.1355A>T
|
ENSP00000443665.1:p.Glu452Val
|
|
|
ENST00000616768.5:c.1022A>T
|
ENSP00000480669.2:p.Glu341Val
|
|
|
ENST00000673673.1:c.1866A>T
|
|
|
|
ENST00000673741.1:n.1112A>T
|
|
|
|
ENST00000673889.1:n.1460A>T
|
|
|
|
ENST00000673897.1:c.*1870A>T
|
ENSP00000501109.1:n.*1870A>T
|
|
|
ENST00000673899.1:c.1346A>T
|
ENSP00000501030.1:p.Glu449Val
|
|
|
ENST00000673947.1:c.*2218A>T
|
ENSP00000501304.1:n.*2218A>T
|
|
|
ENST00000673972.1:c.*1956A>T
|
ENSP00000501281.1:n.*1956A>T
|
|
|
ENST00000674019.1:c.1355A>T
|
ENSP00000501081.1:p.Glu452Val
|
|
|
ENST00000674111.1:c.*307A>T
|
ENSP00000501162.1:n.*307A>T
|
|
|
ENST00000674125.1:n.789A>T
|
|
|
|
ENST00000231790.6:c.2078A>T
|
ENSP00000231790.2:p.Glu693Val
|
|
|
ENST00000413740.1:c.291-1494A>T
|
ENSP00000416476.1:n.291-1494A>T
|
|
|
ENST00000435176.5:c.1784A>T
|
ENSP00000402564.1:p.Glu595Val
|
|
|
ENST00000450420.5:c.182-1494A>T
|
ENSP00000393006.1:n.182-1494A>T
|
|
|
ENST00000455445.6:c.1355A>T
|
ENSP00000398272.2:p.Glu452Val
|
|
|
ENST00000456676.6:c.1871+1309A>T
|
|
|
|
ENST00000458205.6:c.1355A>T
|
ENSP00000402667.2:p.Glu452Val
|
|
|
ENST00000536378.5:c.1355A>T
|
ENSP00000444286.2:p.Glu452Val
|
|
|
ENST00000539477.5:c.1355A>T
|
ENSP00000443665.1:p.Glu452Val
|
|
|
NM_000249.3:c.2078A>T , LRG_216t1:c.2078A>T
|
NP_000240.1:p.Glu693Val
|
|
|
NM_001167617.1:c.1784A>T
|
NP_001161089.1:p.Glu595Val
|
|
|
NM_001167618.1:c.1355A>T
|
NP_001161090.1:p.Glu452Val
|
|
|
NM_001167619.1:c.1355A>T
|
NP_001161091.1:p.Glu452Val
|
|
|
NM_001258271.1:c.1896+1309A>T
|
NP_001245200.1:n.1896+1309A>T
|
|
|
NM_001258273.1:c.1355A>T
|
NP_001245202.1:p.Glu452Val
|
|
|
NM_001258274.1:c.1355A>T
|
NP_001245203.1:p.Glu452Val
|
|
|
XM_005265161.1:c.1871A>T
|
XP_005265218.1:p.Glu624Val
|
|
|
XM_005265163.1:c.1355A>T
|
XP_005265220.1:p.Glu452Val
|
|
|
XM_005265164.1:c.1355A>T
|
XP_005265221.1:p.Glu452Val
|
|
|
XM_005265166.1:c.1055A>T
|
XP_005265223.1:p.Glu352Val
|
|
|
XM_011533727.1:c.1004A>T
|
XP_011532029.1:p.Glu335Val
|
|
|
NM_001167617.2:c.1784A>T
|
NP_001161089.1:p.Glu595Val
|
|
|
NM_001167618.2:c.1355A>T
|
NP_001161090.1:p.Glu452Val
|
|
|
NM_001167619.2:c.1355A>T
|
NP_001161091.1:p.Glu452Val
|
|
|
NM_001258274.2:c.1355A>T
|
NP_001245203.1:p.Glu452Val
|
|
|
NM_001354615.1:c.1355A>T
|
NP_001341544.1:p.Glu452Val
|
|
|
NM_001354616.1:c.1355A>T
|
NP_001341545.1:p.Glu452Val
|
|
|
NM_001354617.1:c.1355A>T
|
NP_001341546.1:p.Glu452Val
|
|
|
NM_001354618.1:c.1355A>T
|
NP_001341547.1:p.Glu452Val
|
|
|
NM_001354619.1:c.1355A>T
|
NP_001341548.1:p.Glu452Val
|
|
|
NM_001354620.1:c.1784A>T
|
NP_001341549.1:p.Glu595Val
|
|
|
NM_001354621.1:c.1055A>T
|
NP_001341550.1:p.Glu352Val
|
|
|
NM_001354622.1:c.1055A>T
|
NP_001341551.1:p.Glu352Val
|
|
|
NM_001354623.1:c.1055A>T
|
NP_001341552.1:p.Glu352Val
|
|
|
NM_001354624.1:c.1004A>T
|
NP_001341553.1:p.Glu335Val
|
|
|
NM_001354625.1:c.1004A>T
|
NP_001341554.1:p.Glu335Val
|
|
|
NM_001354626.1:c.1004A>T
|
NP_001341555.1:p.Glu335Val
|
|
|
NM_001354627.1:c.1004A>T
|
NP_001341556.1:p.Glu335Val
|
|
|
NM_001354628.1:c.1985A>T
|
NP_001341557.1:p.Glu662Val
|
|
|
NM_001354629.1:c.1979A>T
|
NP_001341558.1:p.Glu660Val
|
|
|
NM_001354630.1:c.1913A>T
|
NP_001341559.1:p.Glu638Val
|
|
|
XM_005265161.2:c.1871A>T
|
XP_005265218.1:p.Glu624Val
|
|
|
XM_017006450.2:c.1055A>T
|
XP_016861939.1:p.Glu352Val
|
|
|
NM_000249.4:c.2078A>T
MANE Select
|
NP_000240.1:p.Glu693Val
|
|
|
NM_001167617.3:c.1784A>T
|
NP_001161089.1:p.Glu595Val
|
|
|
NM_001167618.3:c.1355A>T
|
NP_001161090.1:p.Glu452Val
|
|
|
NM_001167619.3:c.1355A>T
|
NP_001161091.1:p.Glu452Val
|
|
|
NM_001258271.2:c.1896+1309A>T
|
NP_001245200.1:n.1896+1309A>T
|
|
|
NM_001258273.2:c.1355A>T
|
NP_001245202.1:p.Glu452Val
|
|
|
NM_001258274.3:c.1355A>T
|
NP_001245203.1:p.Glu452Val
|
|
|
NM_001354615.2:c.1355A>T
|
NP_001341544.1:p.Glu452Val
|
|
|
NM_001354616.2:c.1355A>T
|
NP_001341545.1:p.Glu452Val
|
|
|
NM_001354617.2:c.1355A>T
|
NP_001341546.1:p.Glu452Val
|
|
|
NM_001354618.2:c.1355A>T
|
NP_001341547.1:p.Glu452Val
|
|
|
NM_001354619.2:c.1355A>T
|
NP_001341548.1:p.Glu452Val
|
|
|
NM_001354620.2:c.1784A>T
|
NP_001341549.1:p.Glu595Val
|
|
|
NM_001354621.2:c.1055A>T
|
NP_001341550.1:p.Glu352Val
|
|
|
NM_001354622.2:c.1055A>T
|
NP_001341551.1:p.Glu352Val
|
|
|
NM_001354623.2:c.1055A>T
|
NP_001341552.1:p.Glu352Val
|
|
|
NM_001354624.2:c.1004A>T
|
NP_001341553.1:p.Glu335Val
|
|
|
NM_001354625.2:c.1004A>T
|
NP_001341554.1:p.Glu335Val
|
|
|
NM_001354626.2:c.1004A>T
|
NP_001341555.1:p.Glu335Val
|
|
|
NM_001354627.2:c.1004A>T
|
NP_001341556.1:p.Glu335Val
|
|
|
NM_001354628.2:c.1985A>T
|
NP_001341557.1:p.Glu662Val
|
|
|
NM_001354629.2:c.1979A>T
|
NP_001341558.1:p.Glu660Val
|
|
|
NM_001354630.2:c.1913A>T
|
NP_001341559.1:p.Glu638Val
|
|
