|
ENST00000371418.9:c.278T>G
MANE Select
|
ENSP00000360472.4:p.Leu93Arg
|
|
|
ENST00000635953.1:c.278T>G
|
ENSP00000490058.1:p.Leu93Arg
|
|
|
ENST00000636140.1:n.63T>G
|
|
|
|
ENST00000636155.1:c.278T>G
|
ENSP00000490355.1:p.Leu93Arg
|
|
|
ENST00000636232.1:c.*64T>G
|
ENSP00000490325.1:n.*64T>G
|
|
|
ENST00000636683.1:n.33T>G
|
|
|
|
ENST00000636754.1:c.*68T>G
|
ENSP00000489781.1:n.*68T>G
|
|
|
ENST00000636946.1:c.278T>G
|
ENSP00000490654.1:p.Leu93Arg
|
|
|
ENST00000637037.1:c.278T>G
|
ENSP00000490860.1:p.Leu93Arg
|
|
|
ENST00000637347.1:n.148+134T>G
|
|
|
|
ENST00000637611.1:c.278T>G
|
ENSP00000489682.1:p.Leu93Arg
|
|
|
ENST00000637689.1:c.-1094T>G
|
ENSP00000490496.1:n.-1094T>G
|
|
|
ENST00000637925.1:c.278T>G
|
ENSP00000489763.1:p.Leu93Arg
|
|
|
ENST00000638049.1:c.*36T>G
|
ENSP00000490597.1:n.*36T>G
|
|
|
ENST00000371413.4:c.278T>G
|
ENSP00000360467.3:p.Leu93Arg
|
|
|
ENST00000371418.8:c.278T>G
|
ENSP00000360472.4:p.Leu93Arg
|
|
|
ENST00000478763.2:c.278T>G
|
ENSP00000486517.1:p.Leu93Arg
|
|
|
ENST00000627420.2:c.*68T>G
|
ENSP00000487116.1:n.*68T>G
|
|
|
ENST00000627699.1:c.*68T>G
|
ENSP00000485868.1:n.*68T>G
|
|
|
ENST00000629035.2:c.215+463T>G
|
ENSP00000486908.1:n.215+463T>G
|
|
|
ENST00000630047.2:c.278T>G
|
ENSP00000485917.1:p.Leu93Arg
|
|
|
ENST00000630184.2:c.278T>G
|
ENSP00000486607.1:p.Leu93Arg
|
|
|
ENST00000630487.2:c.*68T>G
|
ENSP00000486859.1:n.*68T>G
|
|
|
NM_001308275.1:c.278T>G
|
NP_001295204.1:p.Leu93Arg
|
|
|
NM_001308276.1:c.278T>G
|
NP_001295205.1:p.Leu93Arg
|
|
|
NM_005097.2:c.278T>G
|
NP_005088.1:p.Leu93Arg
|
|
|
NM_005097.3:c.278T>G
|
NP_005088.1:p.Leu93Arg
|
|
|
NR_131777.1:n.623T>G
|
|
|
|
XM_017016911.2:c.278T>G
|
XP_016872400.1:p.Leu93Arg
|
|
|
XM_017016912.2:c.278T>G
|
XP_016872401.1:p.Leu93Arg
|
|
|
NM_005097.4:c.278T>G
MANE Select
|
NP_005088.1:p.Leu93Arg
|
|
|
NM_001308275.2:c.278T>G
|
NP_001295204.1:p.Leu93Arg
|
|
|
NM_001308276.2:c.278T>G
|
NP_001295205.1:p.Leu93Arg
|
|
|
NR_131777.2:n.496T>G
|
|
|
