|
ENST00000395796.8:c.*1318G>T
|
ENSP00000379142.4:n.*1318G>T
|
|
|
ENST00000616242.5:c.*440G>T
|
ENSP00000482149.2:n.*440G>T
|
|
|
ENST00000683378.1:n.546G>T
|
|
|
|
ENST00000336642.9:c.354G>T
|
ENSP00000338009.5:p.Glu118Asp
|
|
|
ENST00000345378.7:c.1323G>T
|
ENSP00000223366.2:p.Glu441Asp
|
|
|
ENST00000403799.8:c.1320G>T
MANE Select
|
ENSP00000384247.3:p.Glu440Asp
|
|
|
ENST00000671824.1:c.1383G>T
|
ENSP00000500264.1:p.Glu461Asp
|
|
|
ENST00000672743.1:n.332G>T
|
|
|
|
ENST00000673284.1:c.1320G>T
|
ENSP00000499852.1:p.Glu440Asp
|
|
|
ENST00000336642.8:c.372G>T
|
ENSP00000338009.4:p.Glu124Asp
|
|
|
ENST00000345378.6:c.1323G>T
|
ENSP00000223366.2:p.Glu441Asp
|
|
|
ENST00000395796.7:c.1317G>T
|
ENSP00000379142.3:p.Glu439Asp
|
|
|
ENST00000403799.7:c.1320G>T
|
ENSP00000384247.3:p.Glu440Asp
|
|
|
ENST00000437084.1:c.1269G>T
|
ENSP00000402840.1:p.Glu423Asp
|
|
|
ENST00000459642.1:n.700G>T
|
|
|
|
ENST00000616242.4:c.1317G>T
|
ENSP00000482149.1:p.Glu439Asp
|
|
|
NM_000162.3:c.1320G>T
|
NP_000153.1:p.Glu440Asp
|
|
|
NM_033507.1:c.1323G>T
|
NP_277042.1:p.Glu441Asp
|
|
|
NM_033508.1:c.1317G>T
|
NP_277043.1:p.Glu439Asp
|
|
|
NM_000162.4:c.1320G>T
|
NP_000153.1:p.Glu440Asp
|
|
|
NM_001354800.1:c.1320G>T
|
NP_001341729.1:p.Glu440Asp
|
|
|
NM_001354801.1:c.309G>T
|
NP_001341730.1:p.Glu103Asp
|
|
|
NM_001354802.1:c.180G>T
|
NP_001341731.1:p.Glu60Asp
|
|
|
NM_001354803.1:c.354G>T
|
NP_001341732.1:p.Glu118Asp
|
|
|
NM_033507.2:c.1323G>T
|
NP_277042.1:p.Glu441Asp
|
|
|
NM_033508.2:c.1317G>T
|
NP_277043.1:p.Glu439Asp
|
|
|
XM_024446707.1:c.180G>T
|
XP_024302475.1:p.Glu60Asp
|
|
|
NM_000162.5:c.1320G>T
MANE Select
|
NP_000153.1:p.Glu440Asp
|
|
|
NM_033507.3:c.1323G>T
|
NP_277042.1:p.Glu441Asp
|
|
|
NM_033508.3:c.1317G>T
|
NP_277043.1:p.Glu439Asp
|
|
|
NM_001354803.2:c.354G>T
|
NP_001341732.1:p.Glu118Asp
|
|
