ENST00000682073.1:n.2047_2048del
|
|
|
ENST00000682453.1:c.3307_3308del
|
ENSP00000506943.1:p.Ile1103Ter
|
|
ENST00000682477.1:c.*2733_*2734del
|
ENSP00000507075.1:n.*2733_*2734del
|
|
ENST00000682589.1:n.9184_9185del
|
|
|
ENST00000682755.1:c.3085_3086del
|
ENSP00000507660.1:p.Ile1029Ter
|
|
ENST00000682989.1:c.*398_*399del
|
ENSP00000507786.1:n.*398_*399del
|
|
ENST00000683039.1:c.3307_3308del
|
ENSP00000508303.1:p.Ile1103Ter
|
|
ENST00000683235.1:c.*722_*723del
|
ENSP00000507646.1:n.*722_*723del
|
|
ENST00000683535.1:n.1437_1438del
|
|
|
ENST00000684584.1:c.2470_2471del
|
ENSP00000508044.1:p.Ile824Ter
|
|
ENST00000684626.1:n.1553_1554del
|
|
|
ENST00000684769.1:c.1497_1498del
|
ENSP00000507691.1:n.1497_1498del
|
|
ENST00000259008.7:c.3307_3308del
MANE Select
|
ENSP00000259008.2:p.Ile1103Ter
|
|
ENST00000259008.6:c.3307_3308del
|
ENSP00000259008.2:p.Ile1103Ter
|
|
NM_032043.2:c.3307_3308del , LRG_300t1:c.3307_3308del
|
NP_114432.2:p.Ile1103Ter
|
|
XM_011525332.1:c.3367_3368del
|
XP_011523634.1:p.Ile1123Ter
|
|
XM_011525333.1:c.3367_3368del
|
XP_011523635.1:p.Ile1123Ter
|
|
XM_011525334.1:c.3367_3368del
|
XP_011523636.1:p.Ile1123Ter
|
|
XM_011525335.1:c.3307_3308del
|
XP_011523637.1:p.Ile1103Ter
|
|
XM_011525336.1:c.3247_3248del
|
XP_011523638.1:p.Ile1083Ter
|
|
XM_011525337.1:c.3166_3167del
|
XP_011523639.1:p.Ile1056Ter
|
|
XM_011525338.1:c.2884_2885del
|
XP_011523640.1:p.Ile962Ter
|
|
XM_011525332.3:c.3367_3368del
|
XP_011523634.1:p.Ile1123Ter
|
|
XM_011525333.3:c.3367_3368del
|
XP_011523635.1:p.Ile1123Ter
|
|
XM_011525334.2:c.3367_3368del
|
XP_011523636.1:p.Ile1123Ter
|
|
XM_011525335.3:c.3307_3308del
|
XP_011523637.1:p.Ile1103Ter
|
|
XM_011525336.2:c.3247_3248del
|
XP_011523638.1:p.Ile1083Ter
|
|
XM_011525337.2:c.3166_3167del
|
XP_011523639.1:p.Ile1056Ter
|
|
XM_011525338.2:c.2884_2885del
|
XP_011523640.1:p.Ile962Ter
|
|
XM_017025200.1:c.2824_2825del
|
XP_016880689.1:p.Ile942Ter
|
|
XM_017025201.1:c.2824_2825del
|
XP_016880690.1:p.Ile942Ter
|
|
XM_017025202.1:c.1453_1454del
|
XP_016880691.1:p.Ile485Ter
|
|
XM_017025203.1:c.1453_1454del
|
XP_016880692.1:p.Ile485Ter
|
|
NM_032043.3:c.3307_3308del
MANE Select
|
NP_114432.2:p.Ile1103Ter
|
|