ENST00000377313.7:c.1419G>T
|
ENSP00000366530.1:p.Glu473Asp
|
|
ENST00000394374.8:c.*712G>T
|
ENSP00000377899.4:n.*712G>T
|
|
ENST00000394376.7:c.1395G>T
|
ENSP00000377901.3:p.Glu465Asp
|
|
ENST00000413626.2:c.1404G>T
|
ENSP00000411218.2:p.Glu468Asp
|
|
ENST00000424912.2:c.1404G>T
|
ENSP00000388016.2:p.Glu468Asp
|
|
ENST00000429702.6:c.1404G>T
|
ENSP00000402752.2:p.Glu468Asp
|
|
ENST00000672079.2:c.*500G>T
|
ENSP00000500905.2:n.*500G>T
|
|
ENST00000710881.1:c.1419G>T
|
ENSP00000518530.1:p.Glu473Asp
|
|
ENST00000394374.7:c.1151G>T
|
|
|
ENST00000394376.6:c.746G>T
|
|
|
ENST00000478548.3:n.1897G>T
|
|
|
ENST00000671939.2:n.1366G>T
|
|
|
ENST00000671965.2:n.1786G>T
|
|
|
ENST00000312049.11:c.1404G>T
|
ENSP00000308975.6:p.Glu468Asp
|
|
ENST00000315422.9:c.1404G>T
|
ENSP00000323747.4:p.Glu468Asp
|
|
ENST00000377313.6:c.1419G>T
|
ENSP00000366530.1:p.Glu473Asp
|
|
ENST00000440873.6:c.1404G>T
|
ENSP00000413944.2:p.Glu468Asp
|
|
ENST00000450708.7:c.1404G>T
MANE Select
|
ENSP00000394933.3:p.Glu468Asp
|
|
ENST00000478548.2:n.1905G>T
|
|
|
ENST00000671939.1:n.1681G>T
|
|
|
ENST00000672304.1:c.1530G>T
|
ENSP00000500585.1:p.Glu510Asp
|
|
ENST00000312049.10:c.1404G>T
|
ENSP00000308975.6:p.Glu468Asp
|
|
ENST00000315422.8:c.1404G>T
|
ENSP00000323747.4:p.Glu468Asp
|
|
ENST00000337652.5:c.1419G>T
|
ENSP00000337088.1:p.Glu473Asp
|
|
ENST00000377313.5:c.1419G>T
|
ENSP00000366530.1:p.Glu473Asp
|
|
ENST00000377316.6:c.1239G>T
|
ENSP00000366533.1:p.Glu413Asp
|
|
ENST00000377321.5:c.1299G>T
|
ENSP00000366538.1:p.Glu433Asp
|
|
ENST00000377326.7:c.1404G>T
|
ENSP00000366543.3:p.Glu468Asp
|
|
ENST00000394374.6:c.1419G>T
|
ENSP00000377899.2:p.Glu473Asp
|
|
ENST00000394376.5:c.1419G>T
|
ENSP00000377901.1:p.Glu473Asp
|
|
ENST00000478548.1:n.953G>T
|
|
|
NM_000244.3:c.1419G>T , LRG_509t1:c.1419G>T
|
NP_000235.2:p.Glu473Asp
|
|
NM_130799.2:c.1404G>T , LRG_509t2:c.1404G>T
|
NP_570711.1:p.Glu468Asp
|
|
NM_130800.2:c.1419G>T
|
NP_570712.1:p.Glu473Asp
|
|
NM_130801.2:c.1419G>T
|
NP_570713.1:p.Glu473Asp
|
|
NM_130802.2:c.1419G>T
|
NP_570714.1:p.Glu473Asp
|
|
NM_130803.2:c.1419G>T
|
NP_570715.1:p.Glu473Asp
|
|
NM_130804.2:c.1419G>T
|
NP_570716.1:p.Glu473Asp
|
|
XM_005274001.3:c.1404G>T
|
XP_005274058.1:p.Glu468Asp
|
|
XM_011545040.1:c.1530G>T
|
XP_011543342.1:p.Glu510Asp
|
|
XM_011545041.1:c.1530G>T
|
XP_011543343.1:p.Glu510Asp
|
|
XM_011545042.1:c.1530G>T
|
XP_011543344.1:p.Glu510Asp
|
|
XM_005274001.4:c.1404G>T
|
XP_005274058.1:p.Glu468Asp
|
|
XM_011545041.2:c.1530G>T
|
XP_011543343.1:p.Glu510Asp
|
|
XM_011545042.3:c.1530G>T
|
XP_011543344.1:p.Glu510Asp
|
|
XM_017017765.1:c.1545G>T
|
XP_016873254.1:p.Glu515Asp
|
|
XM_017017766.1:c.1545G>T
|
XP_016873255.1:p.Glu515Asp
|
|
XM_017017767.2:c.1545G>T
|
XP_016873256.1:p.Glu515Asp
|
|
XM_017017768.1:c.1545G>T
|
XP_016873257.1:p.Glu515Asp
|
|
XM_017017769.1:c.1404G>T
|
XP_016873258.1:p.Glu468Asp
|
|
XM_017017770.2:c.1404G>T
|
XP_016873259.1:p.Glu468Asp
|
|
NM_001370251.1:c.1530G>T
|
NP_001357180.1:p.Glu510Asp
|
|
NM_001370259.2:c.1404G>T
MANE Select
|
NP_001357188.2:p.Glu468Asp
|
|
NM_001370260.1:c.1404G>T
|
NP_001357189.1:p.Glu468Asp
|
|
NM_001370261.1:c.1404G>T
|
NP_001357190.1:p.Glu468Asp
|
|
NM_001370262.1:c.1299G>T
|
NP_001357191.1:p.Glu433Asp
|
|
NM_001370263.1:c.1299G>T
|
NP_001357192.1:p.Glu433Asp
|
|
NM_000244.4:c.1419G>T
|
NP_000235.3:p.Glu473Asp
|
|
NM_001370251.2:c.1530G>T
|
NP_001357180.2:p.Glu510Asp
|
|
NM_001370260.2:c.1404G>T
|
NP_001357189.2:p.Glu468Asp
|
|
NM_001370261.2:c.1404G>T
|
NP_001357190.2:p.Glu468Asp
|
|
NM_001370262.2:c.1299G>T
|
NP_001357191.2:p.Glu433Asp
|
|
NM_001370263.2:c.1299G>T
|
NP_001357192.2:p.Glu433Asp
|
|
NM_130799.3:c.1404G>T
|
NP_570711.2:p.Glu468Asp
|
|
NM_130800.3:c.1419G>T
|
NP_570712.2:p.Glu473Asp
|
|
NM_130801.3:c.1419G>T
|
NP_570713.2:p.Glu473Asp
|
|
NM_130802.3:c.1419G>T
|
NP_570714.2:p.Glu473Asp
|
|
NM_130803.3:c.1419G>T
|
NP_570715.2:p.Glu473Asp
|
|
NM_130804.3:c.1419G>T
|
NP_570716.2:p.Glu473Asp
|
|