ENST00000700029.2:c.755_756insC
|
ENSP00000514759.2:p.Ile253TyrfsTer?
|
|
ENST00000710265.1:c.755_756insC
|
ENSP00000518161.1:p.Ile253TyrfsTer?
|
|
ENST00000472832.3:c.755_756insC
|
ENSP00000483066.2:p.Ile253TyrfsTer?
|
|
ENST00000688158.2:n.1490_1491insC
|
|
|
ENST00000688922.2:c.*585_*586insC
|
ENSP00000508742.2:n.*585_*586insC
|
|
ENST00000700021.1:c.710_711insC
|
ENSP00000514757.1:p.Ile238TyrfsTer?
|
|
ENST00000700022.1:c.*94_*95insC
|
ENSP00000514758.1:n.*94_*95insC
|
|
ENST00000700023.1:n.1913_1914insC
|
|
|
ENST00000700024.1:n.2147_2148insC
|
|
|
ENST00000700025.1:n.1524_1525insC
|
|
|
ENST00000700026.1:n.392_393insC
|
|
|
ENST00000700029.1:c.589_590insC
|
|
|
ENST00000706954.1:c.755_756insC
|
ENSP00000516674.1:p.Ile253TyrfsTer?
|
|
ENST00000706955.1:c.*790_*791insC
|
ENSP00000516675.1:n.*790_*791insC
|
|
ENST00000686459.1:c.*341_*342insC
|
ENSP00000508909.1:n.*341_*342insC
|
|
ENST00000688158.1:c.*866_*867insC
|
ENSP00000509254.1:n.*866_*867insC
|
|
ENST00000688308.1:c.755_756insC
|
ENSP00000508752.1:p.Ile253TyrfsTer?
|
|
ENST00000688922.1:c.676_677insC
|
|
|
ENST00000693560.1:c.1274_1275insC
|
ENSP00000509861.1:p.Ile426TyrfsTer?
|
|
ENST00000371953.8:c.755_756insC
MANE Select
|
ENSP00000361021.3:p.Ile253TyrfsTer?
|
|
ENST00000371953.7:c.755_756insC
|
ENSP00000361021.3:p.Ile253TyrfsTer?
|
|
ENST00000472832.2:c.182_183insC
|
ENSP00000483066.1:p.Ile62TyrfsTer?
|
|
NM_000314.5:c.755_756insC
|
NP_000305.3:p.Ile253TyrfsTer?
|
|
NM_000314.6:c.755_756insC
|
NP_000305.3:p.Ile253TyrfsTer?
|
|
NM_001304717.2:c.1274_1275insC
|
NP_001291646.2:p.Ile426TyrfsTer?
|
|
NM_001304718.1:c.164_165insC
|
NP_001291647.1:p.Ile56TyrfsTer?
|
|
XM_006717926.2:c.710_711insC
|
XP_006717989.1:p.Ile238TyrfsTer?
|
|
XM_011539981.1:c.755_756insC
|
XP_011538283.1:p.Ile253TyrfsTer?
|
|
XM_011539982.1:c.659_660insC
|
XP_011538284.1:p.Ile221TyrfsTer?
|
|
XR_945791.1:n.1325_1326insC
|
|
|
NM_000314.7:c.755_756insC
|
NP_000305.3:p.Ile253TyrfsTer?
|
|
NM_001304717.5:c.1274_1275insC
|
NP_001291646.4:p.Ile426TyrfsTer?
|
|
NM_001304718.2:c.164_165insC
|
NP_001291647.1:p.Ile56TyrfsTer?
|
|
NM_000314.8:c.755_756insC
MANE Select
|
NP_000305.3:p.Ile253TyrfsTer?
|
|