|
ENST00000689288.1:c.*2421A>G
|
ENSP00000509637.1:n.*2421A>G
|
|
|
ENST00000303395.9:c.4385A>G
|
ENSP00000303540.4:p.Tyr1462Cys
|
|
|
ENST00000635750.1:c.4352A>G
|
ENSP00000490799.1:p.Tyr1451Cys
|
|
|
ENST00000635776.1:c.4352A>G
|
ENSP00000490692.1:p.Tyr1451Cys
|
|
|
ENST00000636194.1:c.*1878A>G
|
ENSP00000490288.1:n.*1878A>G
|
|
|
ENST00000637038.1:c.1247A>G
|
|
|
|
ENST00000637988.1:c.4352A>G
|
ENSP00000490780.1:p.Tyr1451Cys
|
|
|
ENST00000640036.1:c.4352A>G
|
ENSP00000491573.1:p.Tyr1451Cys
|
|
|
ENST00000641575.1:c.4349A>G
|
ENSP00000492917.1:p.Tyr1450Cys
|
|
|
ENST00000641603.1:c.4103A>G
|
ENSP00000492945.1:p.Tyr1368Cys
|
|
|
ENST00000641996.1:c.*3939A>G
|
ENSP00000493054.1:n.*3939A>G
|
|
|
ENST00000671940.1:c.*2328A>G
|
ENSP00000500336.1:n.*2328A>G
|
|
|
ENST00000673490.1:n.6858A>G
|
|
|
|
ENST00000674923.1:c.4385A>G
MANE Select
|
ENSP00000501589.1:p.Tyr1462Cys
|
|
|
ENST00000303395.8:c.4385A>G
|
ENSP00000303540.4:p.Tyr1462Cys
|
|
|
ENST00000375405.7:c.4352A>G
|
ENSP00000364554.3:p.Tyr1451Cys
|
|
|
ENST00000409050.1:c.4301A>G
|
ENSP00000386312.1:p.Tyr1434Cys
|
|
|
ENST00000423058.6:c.4385A>G
|
ENSP00000407030.2:p.Tyr1462Cys
|
|
|
ENST00000473295.2:n.388A>G
|
|
|
|
ENST00000491429.1:n.538A>G
|
|
|
|
NM_001165963.1:c.4385A>G
|
NP_001159435.1:p.Tyr1462Cys
|
|
|
NM_001165964.1:c.4301A>G
|
NP_001159436.1:p.Tyr1434Cys
|
|
|
NM_001202435.1:c.4385A>G
|
NP_001189364.1:p.Tyr1462Cys
|
|
|
NM_006920.4:c.4352A>G , LRG_8t1:c.4352A>G
|
NP_008851.3:p.Tyr1451Cys
|
|
|
NR_110598.1:n.176-17484T>C
|
|
|
|
XM_011511598.1:c.4385A>G
|
XP_011509900.1:p.Tyr1462Cys
|
|
|
XM_011511599.1:c.4385A>G
|
XP_011509901.1:p.Tyr1462Cys
|
|
|
XM_011511600.1:c.4385A>G
|
XP_011509902.1:p.Tyr1462Cys
|
|
|
XM_011511601.1:c.4385A>G
|
XP_011509903.1:p.Tyr1462Cys
|
|
|
XM_011511602.1:c.4385A>G
|
XP_011509904.1:p.Tyr1462Cys
|
|
|
XM_011511603.1:c.4382A>G
|
XP_011509905.1:p.Tyr1461Cys
|
|
|
XM_011511604.1:c.4352A>G
|
XP_011509906.1:p.Tyr1451Cys
|
|
|
XM_011511605.1:c.4349A>G
|
XP_011509907.1:p.Tyr1450Cys
|
|
|
XM_011511606.1:c.4301A>G
|
XP_011509908.1:p.Tyr1434Cys
|
|
|
XM_011511607.1:c.4103A>G
|
XP_011509909.1:p.Tyr1368Cys
|
|
|
XR_922981.1:n.4633A>G
|
|
|
|
NM_001165963.2:c.4385A>G
|
NP_001159435.1:p.Tyr1462Cys
|
|
|
NM_001165964.2:c.4301A>G
|
NP_001159436.1:p.Tyr1434Cys
|
|
|
NM_001202435.2:c.4385A>G
|
NP_001189364.1:p.Tyr1462Cys
|
|
|
NM_001353948.1:c.4385A>G
|
NP_001340877.1:p.Tyr1462Cys
|
|
|
NM_001353949.1:c.4352A>G
|
NP_001340878.1:p.Tyr1451Cys
|
|
|
NM_001353950.1:c.4352A>G
|
NP_001340879.1:p.Tyr1451Cys
|
|
|
NM_001353951.1:c.4352A>G
|
NP_001340880.1:p.Tyr1451Cys
|
|
|
NM_001353952.1:c.4352A>G
|
NP_001340881.1:p.Tyr1451Cys
|
|
|
NM_001353954.1:c.4349A>G
|
NP_001340883.1:p.Tyr1450Cys
|
|
|
NM_001353955.1:c.4349A>G
|
NP_001340884.1:p.Tyr1450Cys
|
|
|
NM_001353957.1:c.4301A>G
|
NP_001340886.1:p.Tyr1434Cys
|
|
|
NM_001353958.1:c.4301A>G
|
NP_001340887.1:p.Tyr1434Cys
|
|
|
NM_001353960.1:c.4298A>G
|
NP_001340889.1:p.Tyr1433Cys
|
|
|
NM_001353961.1:c.1943A>G
|
NP_001340890.1:p.Tyr648Cys
|
|
|
NM_006920.5:c.4352A>G
|
NP_008851.3:p.Tyr1451Cys
|
|
|
NR_148667.1:n.4821A>G
|
|
|
|
XR_001738883.1:n.4835A>G
|
|
|
|
XR_001738884.1:n.4807A>G
|
|
|
|
NM_001165963.3:c.4385A>G
|
NP_001159435.1:p.Tyr1462Cys
|
|
|
NM_001165964.3:c.4301A>G
|
NP_001159436.1:p.Tyr1434Cys
|
|
|
NM_001202435.3:c.4385A>G
|
NP_001189364.1:p.Tyr1462Cys
|
|
|
NM_001353948.2:c.4385A>G
|
NP_001340877.1:p.Tyr1462Cys
|
|
|
NM_001353949.2:c.4352A>G
|
NP_001340878.1:p.Tyr1451Cys
|
|
|
NM_001353950.2:c.4352A>G
|
NP_001340879.1:p.Tyr1451Cys
|
|
|
NM_001353951.2:c.4352A>G
|
NP_001340880.1:p.Tyr1451Cys
|
|
|
NM_001353952.2:c.4352A>G
|
NP_001340881.1:p.Tyr1451Cys
|
|
|
NM_001353954.2:c.4349A>G
|
NP_001340883.1:p.Tyr1450Cys
|
|
|
NM_001353955.2:c.4349A>G
|
NP_001340884.1:p.Tyr1450Cys
|
|
|
NM_001353957.2:c.4301A>G
|
NP_001340886.1:p.Tyr1434Cys
|
|
|
NM_001353958.2:c.4301A>G
|
NP_001340887.1:p.Tyr1434Cys
|
|
|
NM_001353960.2:c.4298A>G
|
NP_001340889.1:p.Tyr1433Cys
|
|
|
NM_001353961.2:c.1943A>G
|
NP_001340890.1:p.Tyr648Cys
|
|
|
NM_006920.6:c.4352A>G
|
NP_008851.3:p.Tyr1451Cys
|
|
|
NR_148667.2:n.4802A>G
|
|
|
|
NM_001165963.4:c.4385A>G
MANE Select
|
NP_001159435.1:p.Tyr1462Cys
|
|
