ENST00000478995.2:n.3311_3312insA
|
|
|
ENST00000488970.2:n.3950_3951insA
|
|
|
ENST00000695614.1:c.1794_1795insA
|
ENSP00000512053.1:p.Glu599ArgfsTer5
|
|
ENST00000695615.1:c.1794_1795insA
|
ENSP00000512054.1:p.Glu599ArgfsTer5
|
|
ENST00000695616.1:c.*1639_*1640insA
|
ENSP00000512055.1:n.*1639_*1640insA
|
|
ENST00000695617.1:c.1791_1792insA
|
ENSP00000512056.1:p.Glu598ArgfsTer5
|
|
ENST00000695618.1:c.*1543_*1544insA
|
ENSP00000512058.1:n.*1543_*1544insA
|
|
ENST00000695619.1:c.*1504_*1505insA
|
ENSP00000512059.1:n.*1504_*1505insA
|
|
ENST00000695620.1:c.*1720_*1721insA
|
ENSP00000512060.1:n.*1720_*1721insA
|
|
ENST00000695621.1:c.*219_*220insA
|
ENSP00000512061.1:n.*219_*220insA
|
|
ENST00000695622.1:c.1731_1732insA
|
ENSP00000512062.1:p.Glu578ArgfsTer5
|
|
ENST00000695623.1:c.1788_1789insA
|
ENSP00000512063.1:p.Glu597ArgfsTer5
|
|
ENST00000695624.1:n.1099_1100insA
|
|
|
ENST00000695625.1:c.1794_1795insA
|
ENSP00000512064.1:p.Glu599ArgfsTer5
|
|
ENST00000695626.1:c.549_550insA
|
ENSP00000512065.1:n.549_550insA
|
|
ENST00000695627.1:c.742_743insA
|
ENSP00000512066.1:n.742_743insA
|
|
ENST00000695628.1:c.353_354insA
|
ENSP00000512067.1:n.353_354insA
|
|
ENST00000695629.1:c.234_235insA
|
ENSP00000512068.1:p.Glu79ArgfsTer5
|
|
ENST00000695630.1:c.521_522insA
|
|
|
ENST00000695631.1:c.115-60_115-59insA
|
|
|
ENST00000703407.1:c.1266_1267insA
|
ENSP00000512057.1:p.Glu423ArgfsTer5
|
|
ENST00000308731.8:c.1794_1795insA
MANE Select
|
ENSP00000308176.8:p.Glu599ArgfsTer5
|
|
ENST00000308731.7:c.1794_1795insA
|
ENSP00000308176.7:p.Glu599ArgfsTer5
|
|
ENST00000372880.5:c.1266_1267insA
|
ENSP00000361971.1:p.Glu423ArgfsTer5
|
|
ENST00000470069.1:n.159_160insA
|
|
|
ENST00000618050.4:c.1793_1794insA
|
ENSP00000479125.1:n.1793_1794insA
|
|
ENST00000621635.4:c.1896_1897insA
|
ENSP00000483570.1:p.Glu633ArgfsTer5
|
|
NM_000061.2:c.1794_1795insA , LRG_128t1:c.1794_1795insA
|
NP_000052.1:p.Glu599ArgfsTer5
|
|
NM_001287344.1:c.1896_1897insA
|
NP_001274273.1:p.Glu633ArgfsTer5
|
|
NM_001287345.1:c.1266_1267insA
|
NP_001274274.1:p.Glu423ArgfsTer5
|
|
NM_000061.3:c.1794_1795insA
MANE Select
|
NP_000052.1:p.Glu599ArgfsTer5
|
|
NM_001287344.2:c.1896_1897insA
|
NP_001274273.1:p.Glu633ArgfsTer5
|
|
NM_001287345.2:c.1266_1267insA
|
NP_001274274.1:p.Glu423ArgfsTer5
|
|