ENST00000682073.1:n.2151_2152delinsCC
|
|
|
ENST00000682453.1:c.3411_3412delinsCC
|
ENSP00000506943.1:p.Asp1138His
|
|
ENST00000682477.1:c.*2837_*2838delinsCC
|
ENSP00000507075.1:n.*2837_*2838delinsCC
|
|
ENST00000682589.1:n.9288_9289delinsCC
|
|
|
ENST00000682755.1:c.3189_3190delinsCC
|
ENSP00000507660.1:p.Asp1064His
|
|
ENST00000682989.1:c.*502_*503delinsCC
|
ENSP00000507786.1:n.*502_*503delinsCC
|
|
ENST00000683039.1:c.3411_3412delinsCC
|
ENSP00000508303.1:p.Asp1138His
|
|
ENST00000683235.1:c.*826_*827delinsCC
|
ENSP00000507646.1:n.*826_*827delinsCC
|
|
ENST00000683535.1:n.1541_1542delinsCC
|
|
|
ENST00000684584.1:c.2574_2575delinsCC
|
ENSP00000508044.1:p.Asp859His
|
|
ENST00000684626.1:n.1657_1658delinsCC
|
|
|
ENST00000684769.1:c.1601_1602delinsCC
|
ENSP00000507691.1:n.1601_1602delinsCC
|
|
ENST00000259008.7:c.3411_3412delinsCC
MANE Select
|
ENSP00000259008.2:p.Asp1138His
|
|
ENST00000259008.6:c.3411_3412delinsCC
|
ENSP00000259008.2:p.Asp1138His
|
|
NM_032043.2:c.3411_3412delinsCC , LRG_300t1:c.3411_3412delinsCC
|
NP_114432.2:p.Asp1138His
|
|
XM_011525332.1:c.3471_3472delinsCC
|
XP_011523634.1:p.Asp1158His
|
|
XM_011525333.1:c.3471_3472delinsCC
|
XP_011523635.1:p.Asp1158His
|
|
XM_011525334.1:c.3471_3472delinsCC
|
XP_011523636.1:p.Asp1158His
|
|
XM_011525335.1:c.3411_3412delinsCC
|
XP_011523637.1:p.Asp1138His
|
|
XM_011525336.1:c.3351_3352delinsCC
|
XP_011523638.1:p.Asp1118His
|
|
XM_011525337.1:c.3270_3271delinsCC
|
XP_011523639.1:p.Asp1091His
|
|
XM_011525338.1:c.2988_2989delinsCC
|
XP_011523640.1:p.Asp997His
|
|
XM_011525332.3:c.3471_3472delinsCC
|
XP_011523634.1:p.Asp1158His
|
|
XM_011525333.3:c.3471_3472delinsCC
|
XP_011523635.1:p.Asp1158His
|
|
XM_011525334.2:c.3471_3472delinsCC
|
XP_011523636.1:p.Asp1158His
|
|
XM_011525335.3:c.3411_3412delinsCC
|
XP_011523637.1:p.Asp1138His
|
|
XM_011525336.2:c.3351_3352delinsCC
|
XP_011523638.1:p.Asp1118His
|
|
XM_011525337.2:c.3270_3271delinsCC
|
XP_011523639.1:p.Asp1091His
|
|
XM_011525338.2:c.2988_2989delinsCC
|
XP_011523640.1:p.Asp997His
|
|
XM_017025200.1:c.2928_2929delinsCC
|
XP_016880689.1:p.Asp977His
|
|
XM_017025201.1:c.2928_2929delinsCC
|
XP_016880690.1:p.Asp977His
|
|
XM_017025202.1:c.1557_1558delinsCC
|
XP_016880691.1:p.Asp520His
|
|
XM_017025203.1:c.1557_1558delinsCC
|
XP_016880692.1:p.Asp520His
|
|
NM_032043.3:c.3411_3412delinsCC
MANE Select
|
NP_114432.2:p.Asp1138His
|
|