ENST00000478995.2:n.1478G>T
|
|
|
ENST00000488970.2:n.1476G>T
|
|
|
ENST00000695614.1:c.1318G>T
|
ENSP00000512053.1:p.Asp440Tyr
|
|
ENST00000695615.1:c.1318G>T
|
ENSP00000512054.1:p.Asp440Tyr
|
|
ENST00000695616.1:c.*1163G>T
|
ENSP00000512055.1:n.*1163G>T
|
|
ENST00000695617.1:c.1315G>T
|
ENSP00000512056.1:p.Asp439Tyr
|
|
ENST00000695618.1:c.*1067G>T
|
ENSP00000512058.1:n.*1067G>T
|
|
ENST00000695619.1:c.*1028G>T
|
ENSP00000512059.1:n.*1028G>T
|
|
ENST00000695620.1:c.*1163G>T
|
ENSP00000512060.1:n.*1163G>T
|
|
ENST00000695621.1:c.1318G>T
|
ENSP00000512061.1:p.Asp440Tyr
|
|
ENST00000695622.1:c.1255G>T
|
ENSP00000512062.1:p.Asp419Tyr
|
|
ENST00000695623.1:c.1312G>T
|
ENSP00000512063.1:p.Asp438Tyr
|
|
ENST00000695624.1:n.623G>T
|
|
|
ENST00000695625.1:c.1318G>T
|
ENSP00000512064.1:p.Asp440Tyr
|
|
ENST00000695626.1:c.290G>T
|
ENSP00000512065.1:n.290G>T
|
|
ENST00000695627.1:c.331G>T
|
ENSP00000512066.1:p.Asp111Tyr
|
|
ENST00000695628.1:c.190+694G>T
|
ENSP00000512067.1:n.190+694G>T
|
|
ENST00000695629.1:c.190+694G>T
|
ENSP00000512068.1:n.190+694G>T
|
|
ENST00000695630.1:c.327G>T
|
|
|
ENST00000695631.1:c.114+1495G>T
|
|
|
ENST00000695632.1:n.335G>T
|
|
|
ENST00000703407.1:c.1038+1559G>T
|
ENSP00000512057.1:n.1038+1559G>T
|
|
ENST00000308731.8:c.1318G>T
MANE Select
|
ENSP00000308176.8:p.Asp440Tyr
|
|
ENST00000308731.7:c.1318G>T
|
ENSP00000308176.7:p.Asp440Tyr
|
|
ENST00000372880.5:c.1038+1559G>T
|
ENSP00000361971.1:n.1038+1559G>T
|
|
ENST00000470329.1:n.268G>T
|
|
|
ENST00000618050.4:c.1318G>T
|
ENSP00000479125.1:p.Asp440Tyr
|
|
ENST00000621635.4:c.1420G>T
|
ENSP00000483570.1:p.Asp474Tyr
|
|
NM_000061.2:c.1318G>T , LRG_128t1:c.1318G>T
|
NP_000052.1:p.Asp440Tyr
|
|
NM_001287344.1:c.1420G>T
|
NP_001274273.1:p.Asp474Tyr
|
|
NM_001287345.1:c.1038+1559G>T
|
NP_001274274.1:n.1038+1559G>T
|
|
NM_000061.3:c.1318G>T
MANE Select
|
NP_000052.1:p.Asp440Tyr
|
|
NM_001287344.2:c.1420G>T
|
NP_001274273.1:p.Asp474Tyr
|
|
NM_001287345.2:c.1038+1559G>T
|
NP_001274274.1:n.1038+1559G>T
|
|