|
ENST00000684561.1:c.*3015C>T
|
ENSP00000506816.1:n.*3015C>T
|
|
|
ENST00000360184.10:c.11556C>T
MANE Select
|
ENSP00000348965.4:p.His3852=
|
|
|
ENST00000553701.1:n.347-2738G>A
|
|
|
|
ENST00000556139.2:n.17C>T
|
|
|
|
ENST00000557242.1:n.329-2738G>A
|
|
|
|
ENST00000557551.1:n.112-2738G>A
|
|
|
|
ENST00000643437.1:n.1510C>T
|
|
|
|
ENST00000643829.1:n.1385C>T
|
|
|
|
ENST00000644794.1:n.1675C>T
|
|
|
|
ENST00000644881.2:c.11556C>T
|
ENSP00000495022.2:p.His3852=
|
|
|
ENST00000645039.2:c.11556C>T
|
ENSP00000495220.2:p.His3852=
|
|
|
ENST00000645149.2:c.11409C>T
|
ENSP00000495944.2:p.His3803=
|
|
|
ENST00000645697.1:n.2219C>T
|
|
|
|
ENST00000647204.2:n.797C>T
|
|
|
|
ENST00000647366.1:n.5110C>T
|
|
|
|
ENST00000679486.1:c.11556C>T
|
ENSP00000506688.1:p.His3852=
|
|
|
ENST00000679629.1:c.11556C>T
|
ENSP00000505589.1:p.His3852=
|
|
|
ENST00000679720.1:c.11556C>T
|
ENSP00000505938.1:p.His3852=
|
|
|
ENST00000679910.1:c.*2638C>T
|
ENSP00000506521.1:n.*2638C>T
|
|
|
ENST00000680120.1:c.11556C>T
|
ENSP00000504863.1:p.His3852=
|
|
|
ENST00000680200.1:c.*815C>T
|
ENSP00000506166.1:n.*815C>T
|
|
|
ENST00000680313.1:c.11556C>T
|
ENSP00000506208.1:p.His3852=
|
|
|
ENST00000680423.1:c.*3287C>T
|
ENSP00000505483.1:n.*3287C>T
|
|
|
ENST00000680715.1:c.11556C>T
|
ENSP00000505332.1:p.His3852=
|
|
|
ENST00000681010.1:c.11556C>T
|
ENSP00000505201.1:p.His3852=
|
|
|
ENST00000681066.1:c.11556C>T
|
ENSP00000506344.1:p.His3852=
|
|
|
ENST00000681123.1:c.11556C>T
|
ENSP00000506124.1:p.His3852=
|
|
|
ENST00000681283.1:c.*268C>T
|
ENSP00000505667.1:n.*268C>T
|
|
|
ENST00000681536.1:c.*4755C>T
|
ENSP00000505821.1:n.*4755C>T
|
|
|
ENST00000681574.1:c.11556C>T
|
ENSP00000505523.1:p.His3852=
|
|
|
ENST00000681822.1:c.11556C>T
|
ENSP00000505744.1:p.His3852=
|
|
|
ENST00000360184.8:c.11556C>T
|
ENSP00000348965.4:p.His3852=
|
|
|
ENST00000556139.1:n.17C>T
|
|
|
|
NM_001376.4:c.11556C>T
|
NP_001367.2:p.His3852=
|
|
|
NM_001376.5:c.11556C>T
MANE Select
|
NP_001367.2:p.His3852=
|
|
