ENST00000682424.1:c.772+4_772+5delinsCT
|
ENSP00000507321.1:n.772+4_772+5delinsCT
|
|
ENST00000299427.12:c.886+4_886+5delinsCT
MANE Select
|
ENSP00000299427.6:n.886+4_886+5delinsCT
|
|
ENST00000436873.7:c.313-583_313-582delinsCT
|
|
|
ENST00000524788.2:n.2049_2050delinsCT
|
|
|
ENST00000524903.2:n.2165_2166delinsCT
|
|
|
ENST00000528807.2:n.546_547delinsCT
|
|
|
ENST00000530040.2:n.480-154_480-153delinsCT
|
|
|
ENST00000533371.6:c.157+4_157+5delinsCT
|
ENSP00000437066.1:n.157+4_157+5delinsCT
|
|
ENST00000642892.1:c.157+4_157+5delinsCT
|
ENSP00000494165.1:n.157+4_157+5delinsCT
|
|
ENST00000643439.1:c.*626+4_*626+5delinsCT
|
ENSP00000495849.1:n.*626+4_*626+5delinsCT
|
|
ENST00000643479.1:n.919_920delinsCT
|
|
|
ENST00000643516.1:c.396-154_396-153delinsCT
|
|
|
ENST00000644151.1:n.2329_2330delinsCT
|
|
|
ENST00000644218.1:c.886+4_886+5delinsCT
|
ENSP00000493574.1:n.886+4_886+5delinsCT
|
|
ENST00000644683.1:c.*339+4_*339+5delinsCT
|
ENSP00000494085.1:n.*339+4_*339+5delinsCT
|
|
ENST00000644810.1:c.607+4_607+5delinsCT
|
ENSP00000495895.1:n.607+4_607+5delinsCT
|
|
ENST00000644831.1:n.1062+4_1062+5delinsCT
|
|
|
ENST00000644933.1:c.157+4_157+5delinsCT
|
ENSP00000496133.1:n.157+4_157+5delinsCT
|
|
ENST00000645020.1:n.2180_2181delinsCT
|
|
|
ENST00000645285.1:c.157+4_157+5delinsCT
|
ENSP00000495058.1:n.157+4_157+5delinsCT
|
|
ENST00000645331.1:n.1256_1257delinsCT
|
|
|
ENST00000645620.1:c.157+4_157+5delinsCT
|
ENSP00000493657.1:n.157+4_157+5delinsCT
|
|
ENST00000646777.1:n.1066_1067delinsCT
|
|
|
ENST00000647016.1:n.1366+4_1366+5delinsCT
|
|
|
ENST00000647152.1:c.157+4_157+5delinsCT
|
ENSP00000495893.1:n.157+4_157+5delinsCT
|
|
ENST00000647209.1:c.*755+4_*755+5delinsCT
|
ENSP00000495558.1:n.*755+4_*755+5delinsCT
|
|
ENST00000647346.1:n.1906+4_1906+5delinsCT
|
|
|
ENST00000299427.10:c.886+4_886+5delinsCT
|
ENSP00000299427.6:n.886+4_886+5delinsCT
|
|
ENST00000436873.6:c.451-154_451-153delinsCT
|
ENSP00000398136.2:n.451-154_451-153delinsCT
|
|
ENST00000528807.1:n.440_441delinsCT
|
|
|
ENST00000533371.5:c.157+4_157+5delinsCT
|
ENSP00000437066.1:n.157+4_157+5delinsCT
|
|
ENST00000611494.4:c.886+4_886+5delinsCT
|
ENSP00000484546.1:n.886+4_886+5delinsCT
|
|
NM_000391.3:c.886+4_886+5delinsCT
|
NP_000382.3:n.886+4_886+5delinsCT
|
|
NM_000391.4:c.886+4_886+5delinsCT
MANE Select
|
NP_000382.3:n.886+4_886+5delinsCT
|
|