ENST00000224721.12:c.1258G>C
MANE Select
|
ENSP00000224721.9:p.Asp420His
|
|
ENST00000398809.9:c.1258G>C
|
ENSP00000381789.5:p.Asp420His
|
|
ENST00000442677.4:c.1258G>C
|
ENSP00000388894.3:p.Asp420His
|
|
ENST00000466757.8:c.689G>C
|
|
|
ENST00000643732.1:n.1094G>C
|
|
|
ENST00000646131.1:c.922G>C
|
ENSP00000495098.1:p.Asp308His
|
|
ENST00000224721.10:c.1273G>C
|
ENSP00000224721.8:p.Asp425His
|
|
ENST00000299366.11:c.1258G>C
|
ENSP00000299366.8:p.Asp420His
|
|
ENST00000398809.8:c.1258G>C
|
ENSP00000381789.5:p.Asp420His
|
|
ENST00000398842.7:c.1003G>C
|
ENSP00000381822.4:p.Asp335His
|
|
ENST00000442677.3:c.33G>C
|
|
|
ENST00000461841.7:c.1258G>C
|
ENSP00000473454.2:p.Asp420His
|
|
ENST00000466757.7:c.689G>C
|
|
|
ENST00000470494.5:c.227G>C
|
|
|
ENST00000616684.4:c.1258G>C
|
ENSP00000482036.2:p.Asp420His
|
|
ENST00000622827.4:c.1258G>C
|
ENSP00000483211.1:p.Asp420His
|
|
NM_001171930.1:c.1258G>C
|
NP_001165401.1:p.Asp420His
|
|
NM_001171931.1:c.1258G>C
|
NP_001165402.1:p.Asp420His
|
|
NM_022124.5:c.1258G>C
|
NP_071407.4:p.Asp420His
|
|
NM_052836.3:c.1258G>C
|
NP_443068.1:p.Asp420His
|
|
XM_006717940.2:c.1453G>C
|
XP_006718003.1:p.Asp485His
|
|
XM_006717942.2:c.1387G>C
|
XP_006718005.1:p.Asp463His
|
|
XM_011540039.1:c.1453G>C
|
XP_011538341.1:p.Asp485His
|
|
XM_011540040.1:c.1447G>C
|
XP_011538342.1:p.Asp483His
|
|
XM_011540041.1:c.1393G>C
|
XP_011538343.1:p.Asp465His
|
|
XM_011540042.1:c.1453G>C
|
XP_011538344.1:p.Asp485His
|
|
XM_011540043.1:c.1453G>C
|
XP_011538345.1:p.Asp485His
|
|
XM_011540044.1:c.1318G>C
|
XP_011538346.1:p.Asp440His
|
|
XM_011540045.1:c.1453G>C
|
XP_011538347.1:p.Asp485His
|
|
XM_011540046.1:c.913G>C
|
XP_011538348.1:p.Asp305His
|
|
XM_011540047.1:c.271G>C
|
XP_011538349.1:p.Asp91His
|
|
XM_011540048.1:c.1453G>C
|
XP_011538350.1:p.Asp485His
|
|
XM_011540049.1:c.1453G>C
|
XP_011538351.1:p.Asp485His
|
|
XM_011540050.1:c.1453G>C
|
XP_011538352.1:p.Asp485His
|
|
XM_011540051.1:c.1453G>C
|
XP_011538353.1:p.Asp485His
|
|
XM_011540053.1:c.1453G>C
|
XP_011538355.1:p.Asp485His
|
|
XM_011540054.1:c.1393G>C
|
XP_011538356.1:p.Asp465His
|
|
XR_945796.1:n.1696G>C
|
|
|
NM_001171930.2:c.1258G>C
|
NP_001165401.1:p.Asp420His
|
|
NM_001171931.2:c.1258G>C
|
NP_001165402.1:p.Asp420His
|
|
NM_022124.6:c.1258G>C
MANE Select
|
NP_071407.4:p.Asp420His
|
|
NM_052836.4:c.1258G>C
|
NP_443068.1:p.Asp420His
|
|