|
ENST00000405460.9:c.11552_11553insCACCC
MANE Select
|
ENSP00000384582.2:p.Glu3851AspfsTer29
|
|
|
ENST00000425867.3:c.683_684insCACCC
|
ENSP00000392618.3:p.Glu228AspfsTer27
|
|
|
ENST00000639431.1:c.265+78948_265+78949insCACCC
|
ENSP00000491057.1:n.265+78948_265+78949insCACCC
|
|
|
ENST00000640374.1:n.4696_4697insCACCC
|
|
|
|
ENST00000640464.1:n.1971_1972insCACCC
|
|
|
|
ENST00000405460.6:c.11552_11553insCACCC
|
ENSP00000384582.2:p.Glu3851AspfsTer29
|
|
|
ENST00000509621.1:c.4249_4250insCACCC
|
|
|
|
NM_032119.3:c.11552_11553insCACCC
|
NP_115495.3:p.Glu3851AspfsTer29
|
|
|
NR_003149.1:n.11565_11566insCACCC
|
|
|
|
XM_011543675.1:c.11549_11550insCACCC
|
XP_011541977.1:p.Glu3850AspfsTer29
|
|
|
XM_011543676.1:c.11471_11472insCACCC
|
XP_011541978.1:p.Glu3824AspfsTer29
|
|
|
XM_011543677.1:c.8855_8856insCACCC
|
XP_011541979.1:p.Glu2952AspfsTer29
|
|
|
XM_011543678.1:c.11552_11553insCACCC
|
XP_011541980.1:p.Glu3851AspfsTer29
|
|
|
NM_032119.4:c.11552_11553insCACCC
MANE Select
|
NP_115495.3:p.Glu3851AspfsTer29
|
|
|
XM_017009963.2:c.11573_11574insCACCC
|
XP_016865452.1:p.Glu3858AspfsTer29
|
|
|
XM_017009964.2:c.11570_11571insCACCC
|
XP_016865453.1:p.Glu3857AspfsTer29
|
|
|
XM_017009965.1:c.11570_11571insCACCC
|
XP_016865454.1:p.Glu3857AspfsTer29
|
|
|
XM_017009966.2:c.11492_11493insCACCC
|
XP_016865455.1:p.Glu3831AspfsTer29
|
|
|
XM_017009967.1:c.11477_11478insCACCC
|
XP_016865456.1:p.Glu3826AspfsTer29
|
|
|
XM_017009968.2:c.11573_11574insCACCC
|
XP_016865457.1:p.Glu3858AspfsTer29
|
|
|
XM_017009969.2:c.11573_11574insCACCC
|
XP_016865458.1:p.Glu3858AspfsTer29
|
|
|
XM_017009970.2:c.11573_11574insCACCC
|
XP_016865459.1:p.Glu3858AspfsTer29
|
|
|
XM_017009971.2:c.11573_11574insCACCC
|
XP_016865460.1:p.Glu3858AspfsTer29
|
|
|
XM_017009972.1:c.4691_4692insCACCC
|
XP_016865461.1:p.Glu1564AspfsTer29
|
|
|
XM_017009973.1:c.4670_4671insCACCC
|
XP_016865462.1:p.Glu1557AspfsTer29
|
|
|
NR_003149.2:n.11568_11569insCACCC
|
|
|
