ENST00000224721.12:c.3194C>A
MANE Select
|
ENSP00000224721.9:p.Ala1065Asp
|
|
ENST00000398809.9:c.3194C>A
|
ENSP00000381789.5:p.Ala1065Asp
|
|
ENST00000442677.4:c.3194C>A
|
ENSP00000388894.3:p.Ala1065Asp
|
|
ENST00000466757.8:c.2625C>A
|
|
|
ENST00000224721.10:c.3209C>A
|
ENSP00000224721.8:p.Ala1070Asp
|
|
ENST00000398809.8:c.3194C>A
|
ENSP00000381789.5:p.Ala1065Asp
|
|
ENST00000442677.3:c.1969C>A
|
|
|
ENST00000466757.7:c.2625C>A
|
|
|
ENST00000616684.4:c.3194C>A
|
ENSP00000482036.2:p.Ala1065Asp
|
|
ENST00000622827.4:c.3194C>A
|
ENSP00000483211.1:p.Ala1065Asp
|
|
NM_001171930.1:c.3194C>A
|
NP_001165401.1:p.Ala1065Asp
|
|
NM_022124.5:c.3194C>A
|
NP_071407.4:p.Ala1065Asp
|
|
XM_006717940.2:c.3389C>A
|
XP_006718003.1:p.Ala1130Asp
|
|
XM_006717942.2:c.3323C>A
|
XP_006718005.1:p.Ala1108Asp
|
|
XM_011540039.1:c.3389C>A
|
XP_011538341.1:p.Ala1130Asp
|
|
XM_011540040.1:c.3383C>A
|
XP_011538342.1:p.Ala1128Asp
|
|
XM_011540041.1:c.3329C>A
|
XP_011538343.1:p.Ala1110Asp
|
|
XM_011540042.1:c.3389C>A
|
XP_011538344.1:p.Ala1130Asp
|
|
XM_011540043.1:c.3389C>A
|
XP_011538345.1:p.Ala1130Asp
|
|
XM_011540044.1:c.3254C>A
|
XP_011538346.1:p.Ala1085Asp
|
|
XM_011540045.1:c.3389C>A
|
XP_011538347.1:p.Ala1130Asp
|
|
XM_011540046.1:c.2849C>A
|
XP_011538348.1:p.Ala950Asp
|
|
XM_011540047.1:c.2207C>A
|
XP_011538349.1:p.Ala736Asp
|
|
XM_011540048.1:c.3389C>A
|
XP_011538350.1:p.Ala1130Asp
|
|
XM_011540049.1:c.3389C>A
|
XP_011538351.1:p.Ala1130Asp
|
|
XM_011540050.1:c.3389C>A
|
XP_011538352.1:p.Ala1130Asp
|
|
XM_011540051.1:c.3389C>A
|
XP_011538353.1:p.Ala1130Asp
|
|
XM_011540053.1:c.3389C>A
|
XP_011538355.1:p.Ala1130Asp
|
|
XR_945796.1:n.3632C>A
|
|
|
NM_001171930.2:c.3194C>A
|
NP_001165401.1:p.Ala1065Asp
|
|
NM_022124.6:c.3194C>A
MANE Select
|
NP_071407.4:p.Ala1065Asp
|
|