|
ENST00000224721.12:c.683A>T
MANE Select
|
ENSP00000224721.9:p.Asp228Val
|
|
|
ENST00000398809.9:c.683A>T
|
ENSP00000381789.5:p.Asp228Val
|
|
|
ENST00000442677.4:c.683A>T
|
ENSP00000388894.3:p.Asp228Val
|
|
|
ENST00000466757.8:c.54A>T
|
|
|
|
ENST00000643732.1:n.459A>T
|
|
|
|
ENST00000646131.1:c.347A>T
|
ENSP00000495098.1:p.Asp116Val
|
|
|
ENST00000224721.10:c.698A>T
|
ENSP00000224721.8:p.Asp233Val
|
|
|
ENST00000299366.11:c.683A>T
|
ENSP00000299366.8:p.Asp228Val
|
|
|
ENST00000398809.8:c.683A>T
|
ENSP00000381789.5:p.Asp228Val
|
|
|
ENST00000398842.7:c.461+3A>T
|
ENSP00000381822.4:n.461+3A>T
|
|
|
ENST00000461841.7:c.683A>T
|
ENSP00000473454.2:p.Asp228Val
|
|
|
ENST00000466757.7:c.54A>T
|
|
|
|
ENST00000616684.4:c.683A>T
|
ENSP00000482036.2:p.Asp228Val
|
|
|
ENST00000622827.4:c.683A>T
|
ENSP00000483211.1:p.Asp228Val
|
|
|
NM_001171930.1:c.683A>T
|
NP_001165401.1:p.Asp228Val
|
|
|
NM_001171931.1:c.683A>T
|
NP_001165402.1:p.Asp228Val
|
|
|
NM_001171932.1:c.683A>T
|
NP_001165403.1:p.Asp228Val
|
|
|
NM_022124.5:c.683A>T
|
NP_071407.4:p.Asp228Val
|
|
|
NM_052836.3:c.683A>T
|
NP_443068.1:p.Asp228Val
|
|
|
XM_006717940.2:c.818A>T
|
XP_006718003.1:p.Asp273Val
|
|
|
XM_006717942.2:c.818A>T
|
XP_006718005.1:p.Asp273Val
|
|
|
XM_011540039.1:c.818A>T
|
XP_011538341.1:p.Asp273Val
|
|
|
XM_011540040.1:c.818A>T
|
XP_011538342.1:p.Asp273Val
|
|
|
XM_011540041.1:c.818A>T
|
XP_011538343.1:p.Asp273Val
|
|
|
XM_011540042.1:c.818A>T
|
XP_011538344.1:p.Asp273Val
|
|
|
XM_011540043.1:c.818A>T
|
XP_011538345.1:p.Asp273Val
|
|
|
XM_011540044.1:c.683A>T
|
XP_011538346.1:p.Asp228Val
|
|
|
XM_011540045.1:c.818A>T
|
XP_011538347.1:p.Asp273Val
|
|
|
XM_011540046.1:c.278A>T
|
XP_011538348.1:p.Asp93Val
|
|
|
XM_011540048.1:c.818A>T
|
XP_011538350.1:p.Asp273Val
|
|
|
XM_011540049.1:c.818A>T
|
XP_011538351.1:p.Asp273Val
|
|
|
XM_011540050.1:c.818A>T
|
XP_011538352.1:p.Asp273Val
|
|
|
XM_011540051.1:c.818A>T
|
XP_011538353.1:p.Asp273Val
|
|
|
XM_011540053.1:c.818A>T
|
XP_011538355.1:p.Asp273Val
|
|
|
XM_011540054.1:c.818A>T
|
XP_011538356.1:p.Asp273Val
|
|
|
XR_246128.2:n.162-5714T>A
|
|
|
|
XR_945796.1:n.1061A>T
|
|
|
|
NM_001171930.2:c.683A>T
|
NP_001165401.1:p.Asp228Val
|
|
|
NM_001171931.2:c.683A>T
|
NP_001165402.1:p.Asp228Val
|
|
|
NM_022124.6:c.683A>T
MANE Select
|
NP_071407.4:p.Asp228Val
|
|
|
NM_052836.4:c.683A>T
|
NP_443068.1:p.Asp228Val
|
|
|
NM_001171932.2:c.683A>T
|
NP_001165403.1:p.Asp228Val
|
|
