ENST00000683375.1:c.322G>T
MANE Select
|
ENSP00000506769.1:p.Glu108Ter
|
|
ENST00000414387.6:c.319G>T
|
ENSP00000428248.1:p.Glu107Ter
|
|
ENST00000523374.5:c.337G>T
|
ENSP00000429148.1:p.Glu113Ter
|
|
NM_001039891.2:c.337G>T
|
NP_001034980.1:p.Glu113Ter
|
|
NM_001146291.1:c.319G>T
|
NP_001139763.1:p.Glu107Ter
|
|
NM_001190417.1:c.322G>T
|
NP_001177346.1:p.Glu108Ter
|
|
XM_011543941.1:c.337G>T
|
XP_011542243.1:p.Glu113Ter
|
|
XM_011543942.1:c.337G>T
|
XP_011542244.1:p.Glu113Ter
|
|
XM_011543943.1:c.334G>T
|
XP_011542245.1:p.Glu112Ter
|
|
XM_011543944.1:c.229G>T
|
XP_011542246.1:p.Glu77Ter
|
|
XM_011543945.1:c.136G>T
|
XP_011542247.1:p.Glu46Ter
|
|
XM_011543946.1:c.133G>T
|
XP_011542248.1:p.Glu45Ter
|
|
XM_011543941.3:c.337G>T
|
XP_011542243.1:p.Glu113Ter
|
|
XM_011543943.3:c.334G>T
|
XP_011542245.1:p.Glu112Ter
|
|
XM_011543944.2:c.229G>T
|
XP_011542246.1:p.Glu77Ter
|
|
XM_011543945.2:c.136G>T
|
XP_011542247.1:p.Glu46Ter
|
|
XM_017029728.1:c.136G>T
|
XP_016885217.1:p.Glu46Ter
|
|
XM_017029729.1:c.136G>T
|
XP_016885218.1:p.Glu46Ter
|
|
XM_017029730.2:c.136G>T
|
XP_016885219.1:p.Glu46Ter
|
|
XM_017029731.1:c.136G>T
|
XP_016885220.1:p.Glu46Ter
|
|
XM_017029732.1:c.133G>T
|
XP_016885221.1:p.Glu45Ter
|
|
XM_017029733.2:c.133G>T
|
XP_016885222.1:p.Glu45Ter
|
|
NM_001039891.3:c.337G>T
|
NP_001034980.1:p.Glu113Ter
|
|
NM_001146291.2:c.319G>T
|
NP_001139763.1:p.Glu107Ter
|
|
NM_001190417.2:c.322G>T
MANE Select
|
NP_001177346.1:p.Glu108Ter
|
|