ENST00000700029.2:c.750_751insC
|
ENSP00000514759.2:p.Gly251ArgfsTer2
|
|
ENST00000710265.1:c.750_751insC
|
ENSP00000518161.1:p.Gly251ArgfsTer2
|
|
ENST00000472832.3:c.750_751insC
|
ENSP00000483066.2:p.Gly251ArgfsTer2
|
|
ENST00000688158.2:n.1485_1486insC
|
|
|
ENST00000688922.2:c.*580_*581insC
|
ENSP00000508742.2:n.*580_*581insC
|
|
ENST00000700021.1:c.705_706insC
|
ENSP00000514757.1:p.Gly236ArgfsTer2
|
|
ENST00000700022.1:c.*89_*90insC
|
ENSP00000514758.1:n.*89_*90insC
|
|
ENST00000700023.1:n.1908_1909insC
|
|
|
ENST00000700024.1:n.2142_2143insC
|
|
|
ENST00000700025.1:n.1519_1520insC
|
|
|
ENST00000700026.1:n.387_388insC
|
|
|
ENST00000700029.1:c.584_585insC
|
|
|
ENST00000706954.1:c.750_751insC
|
ENSP00000516674.1:p.Gly251ArgfsTer2
|
|
ENST00000706955.1:c.*785_*786insC
|
ENSP00000516675.1:n.*785_*786insC
|
|
ENST00000686459.1:c.*336_*337insC
|
ENSP00000508909.1:n.*336_*337insC
|
|
ENST00000688158.1:c.*861_*862insC
|
ENSP00000509254.1:n.*861_*862insC
|
|
ENST00000688308.1:c.750_751insC
|
ENSP00000508752.1:p.Gly251ArgfsTer2
|
|
ENST00000688922.1:c.671_672insC
|
|
|
ENST00000693560.1:c.1269_1270insC
|
ENSP00000509861.1:p.Gly424ArgfsTer2
|
|
ENST00000371953.8:c.750_751insC
MANE Select
|
ENSP00000361021.3:p.Gly251ArgfsTer2
|
|
ENST00000371953.7:c.750_751insC
|
ENSP00000361021.3:p.Gly251ArgfsTer2
|
|
ENST00000472832.2:c.177_178insC
|
ENSP00000483066.1:p.Gly60ArgfsTer2
|
|
NM_000314.5:c.750_751insC
|
NP_000305.3:p.Gly251ArgfsTer2
|
|
NM_000314.6:c.750_751insC
|
NP_000305.3:p.Gly251ArgfsTer2
|
|
NM_001304717.2:c.1269_1270insC
|
NP_001291646.2:p.Gly424ArgfsTer2
|
|
NM_001304718.1:c.159_160insC
|
NP_001291647.1:p.Gly54ArgfsTer2
|
|
XM_006717926.2:c.705_706insC
|
XP_006717989.1:p.Gly236ArgfsTer2
|
|
XM_011539981.1:c.750_751insC
|
XP_011538283.1:p.Gly251ArgfsTer2
|
|
XM_011539982.1:c.654_655insC
|
XP_011538284.1:p.Gly219ArgfsTer2
|
|
XR_945791.1:n.1320_1321insC
|
|
|
NM_000314.7:c.750_751insC
|
NP_000305.3:p.Gly251ArgfsTer2
|
|
NM_001304717.5:c.1269_1270insC
|
NP_001291646.4:p.Gly424ArgfsTer2
|
|
NM_001304718.2:c.159_160insC
|
NP_001291647.1:p.Gly54ArgfsTer2
|
|
NM_000314.8:c.750_751insC
MANE Select
|
NP_000305.3:p.Gly251ArgfsTer2
|
|