|
ENST00000371068.11:c.1630G>C
MANE Select
|
ENSP00000360107.4:p.Glu544Gln
|
|
|
ENST00000480623.6:c.1630G>C
|
ENSP00000434498.2:p.Glu544Gln
|
|
|
ENST00000635760.1:c.1306G>C
|
ENSP00000489765.1:p.Glu436Gln
|
|
|
ENST00000635812.1:c.*931G>C
|
ENSP00000490859.1:n.*931G>C
|
|
|
ENST00000635866.1:c.*1499G>C
|
ENSP00000489866.1:n.*1499G>C
|
|
|
ENST00000635911.1:n.3148G>C
|
|
|
|
ENST00000635984.1:c.1306G>C
|
ENSP00000489921.1:p.Glu436Gln
|
|
|
ENST00000635996.1:c.1630G>C
|
ENSP00000490256.1:p.Glu544Gln
|
|
|
ENST00000636107.1:c.1630G>C
|
ENSP00000489680.1:p.Glu544Gln
|
|
|
ENST00000636311.1:n.1524G>C
|
|
|
|
ENST00000636343.1:c.1296G>C
|
|
|
|
ENST00000636379.1:c.1342G>C
|
ENSP00000490622.1:p.Glu448Gln
|
|
|
ENST00000636398.1:c.1330G>C
|
ENSP00000489654.1:n.1330G>C
|
|
|
ENST00000636489.1:c.1573G>C
|
ENSP00000489998.1:p.Glu525Gln
|
|
|
ENST00000636616.1:n.1191G>C
|
|
|
|
ENST00000636702.1:c.1600G>C
|
ENSP00000489623.1:p.Glu534Gln
|
|
|
ENST00000636954.1:c.1573G>C
|
ENSP00000489966.1:p.Glu525Gln
|
|
|
ENST00000637089.1:c.1630G>C
|
ENSP00000489854.1:p.Glu544Gln
|
|
|
ENST00000637121.1:n.1432G>C
|
|
|
|
ENST00000637263.1:c.1630G>C
|
ENSP00000489700.1:p.Glu544Gln
|
|
|
ENST00000637340.1:n.3555G>C
|
|
|
|
ENST00000637353.1:c.1630G>C
|
ENSP00000490441.1:p.Glu544Gln
|
|
|
ENST00000637602.1:c.*1331G>C
|
ENSP00000490074.1:n.*1331G>C
|
|
|
ENST00000637849.1:n.1694G>C
|
|
|
|
ENST00000637892.1:n.1834G>C
|
|
|
|
ENST00000371068.9:c.1630G>C
|
ENSP00000360107.4:p.Glu544Gln
|
|
|
ENST00000480623.5:c.*2050G>C
|
ENSP00000434498.1:n.*2050G>C
|
|
|
ENST00000538167.2:c.1573G>C
|
ENSP00000444521.1:p.Glu525Gln
|
|
|
NM_001172420.1:c.1573G>C
|
NP_001165891.1:p.Glu525Gln
|
|
|
NM_018100.3:c.1630G>C
|
NP_060570.2:p.Glu544Gln
|
|
|
NR_033327.1:n.3102G>C
|
|
|
|
NM_018100.4:c.1630G>C
MANE Select
|
NP_060570.2:p.Glu544Gln
|
|
|
NM_001172420.2:c.1573G>C
|
NP_001165891.1:p.Glu525Gln
|
|
|
NR_033327.2:n.2956G>C
|
|
|
