ENST00000682424.1:c.1090G>T
|
ENSP00000507321.1:p.Glu364Ter
|
|
ENST00000299427.12:c.1204G>T
MANE Select
|
ENSP00000299427.6:p.Glu402Ter
|
|
ENST00000436873.7:c.441G>T
|
|
|
ENST00000524924.2:n.324G>T
|
|
|
ENST00000533371.6:c.475G>T
|
ENSP00000437066.1:p.Glu159Ter
|
|
ENST00000642892.1:c.475G>T
|
ENSP00000494165.1:p.Glu159Ter
|
|
ENST00000643342.1:c.277G>T
|
|
|
ENST00000643439.1:c.*944G>T
|
ENSP00000495849.1:n.*944G>T
|
|
ENST00000643479.1:n.1390G>T
|
|
|
ENST00000643516.1:c.713G>T
|
|
|
ENST00000644218.1:c.1015G>T
|
ENSP00000493574.1:p.Glu339Ter
|
|
ENST00000644683.1:c.*657G>T
|
ENSP00000494085.1:n.*657G>T
|
|
ENST00000644810.1:c.925G>T
|
ENSP00000495895.1:p.Glu309Ter
|
|
ENST00000644831.1:n.1380G>T
|
|
|
ENST00000644933.1:c.*70G>T
|
ENSP00000496133.1:n.*70G>T
|
|
ENST00000645285.1:c.*70G>T
|
ENSP00000495058.1:n.*70G>T
|
|
ENST00000645331.1:n.2409G>T
|
|
|
ENST00000645620.1:c.475G>T
|
ENSP00000493657.1:p.Glu159Ter
|
|
ENST00000646691.1:n.979G>T
|
|
|
ENST00000646777.1:n.1537G>T
|
|
|
ENST00000647016.1:n.1684G>T
|
|
|
ENST00000647152.1:c.475G>T
|
ENSP00000495893.1:p.Glu159Ter
|
|
ENST00000647209.1:c.*1073G>T
|
ENSP00000495558.1:n.*1073G>T
|
|
ENST00000647346.1:n.2224G>T
|
|
|
ENST00000299427.10:c.1204G>T
|
ENSP00000299427.6:p.Glu402Ter
|
|
ENST00000524924.1:n.159G>T
|
|
|
ENST00000532191.1:n.257G>T
|
|
|
ENST00000533371.5:c.475G>T
|
ENSP00000437066.1:p.Glu159Ter
|
|
ENST00000611494.4:c.1204G>T
|
ENSP00000484546.1:p.Glu402Ter
|
|
NM_000391.3:c.1204G>T
|
NP_000382.3:p.Glu402Ter
|
|
NM_000391.4:c.1204G>T
MANE Select
|
NP_000382.3:p.Glu402Ter
|
|