|
ENST00000684561.1:c.*3018A>C
|
ENSP00000506816.1:n.*3018A>C
|
|
|
ENST00000360184.10:c.11559A>C
MANE Select
|
ENSP00000348965.4:p.Thr3853=
|
|
|
ENST00000553701.1:n.347-2741T>G
|
|
|
|
ENST00000556139.2:n.20A>C
|
|
|
|
ENST00000557242.1:n.329-2741T>G
|
|
|
|
ENST00000557551.1:n.112-2741T>G
|
|
|
|
ENST00000643437.1:n.1513A>C
|
|
|
|
ENST00000643829.1:n.1388A>C
|
|
|
|
ENST00000644794.1:n.1678A>C
|
|
|
|
ENST00000644881.2:c.11559A>C
|
ENSP00000495022.2:p.Thr3853=
|
|
|
ENST00000645039.2:c.11559A>C
|
ENSP00000495220.2:p.Thr3853=
|
|
|
ENST00000645149.2:c.11412A>C
|
ENSP00000495944.2:p.Thr3804=
|
|
|
ENST00000645697.1:n.2222A>C
|
|
|
|
ENST00000647204.2:n.800A>C
|
|
|
|
ENST00000647366.1:n.5113A>C
|
|
|
|
ENST00000679486.1:c.11559A>C
|
ENSP00000506688.1:p.Thr3853=
|
|
|
ENST00000679629.1:c.11559A>C
|
ENSP00000505589.1:p.Thr3853=
|
|
|
ENST00000679720.1:c.11559A>C
|
ENSP00000505938.1:p.Thr3853=
|
|
|
ENST00000679910.1:c.*2641A>C
|
ENSP00000506521.1:n.*2641A>C
|
|
|
ENST00000680120.1:c.11559A>C
|
ENSP00000504863.1:p.Thr3853=
|
|
|
ENST00000680200.1:c.*818A>C
|
ENSP00000506166.1:n.*818A>C
|
|
|
ENST00000680313.1:c.11559A>C
|
ENSP00000506208.1:p.Thr3853=
|
|
|
ENST00000680423.1:c.*3290A>C
|
ENSP00000505483.1:n.*3290A>C
|
|
|
ENST00000680715.1:c.11559A>C
|
ENSP00000505332.1:p.Thr3853=
|
|
|
ENST00000681010.1:c.11559A>C
|
ENSP00000505201.1:p.Thr3853=
|
|
|
ENST00000681066.1:c.11559A>C
|
ENSP00000506344.1:p.Thr3853=
|
|
|
ENST00000681123.1:c.11559A>C
|
ENSP00000506124.1:p.Thr3853=
|
|
|
ENST00000681283.1:c.*271A>C
|
ENSP00000505667.1:n.*271A>C
|
|
|
ENST00000681536.1:c.*4758A>C
|
ENSP00000505821.1:n.*4758A>C
|
|
|
ENST00000681574.1:c.11559A>C
|
ENSP00000505523.1:p.Thr3853=
|
|
|
ENST00000681822.1:c.11559A>C
|
ENSP00000505744.1:p.Thr3853=
|
|
|
ENST00000360184.8:c.11559A>C
|
ENSP00000348965.4:p.Thr3853=
|
|
|
ENST00000556139.1:n.20A>C
|
|
|
|
NM_001376.4:c.11559A>C
|
NP_001367.2:p.Thr3853=
|
|
|
NM_001376.5:c.11559A>C
MANE Select
|
NP_001367.2:p.Thr3853=
|
|
