|
ENST00000700029.2:c.737_738insTCGTACCG
|
ENSP00000514759.2:p.Leu247ArgfsTer12
|
|
|
ENST00000710265.1:c.737_738insTCGTACCG
|
ENSP00000518161.1:p.Leu247ArgfsTer12
|
|
|
ENST00000472832.3:c.737_738insTCGTACCG
|
ENSP00000483066.2:p.Leu247ArgfsTer12
|
|
|
ENST00000688158.2:n.1472_1473insTCGTACCG
|
|
|
|
ENST00000688922.2:c.*567_*568insTCGTACCG
|
ENSP00000508742.2:n.*567_*568insTCGTACCG
|
|
|
ENST00000700021.1:c.692_693insTCGTACCG
|
ENSP00000514757.1:p.Leu232ArgfsTer12
|
|
|
ENST00000700022.1:c.*76_*77insTCGTACCG
|
ENSP00000514758.1:n.*76_*77insTCGTACCG
|
|
|
ENST00000700023.1:n.1895_1896insTCGTACCG
|
|
|
|
ENST00000700024.1:n.2129_2130insTCGTACCG
|
|
|
|
ENST00000700025.1:n.1506_1507insTCGTACCG
|
|
|
|
ENST00000700026.1:n.374_375insTCGTACCG
|
|
|
|
ENST00000700029.1:c.571_572insTCGTACCG
|
|
|
|
ENST00000706954.1:c.737_738insTCGTACCG
|
ENSP00000516674.1:p.Leu247ArgfsTer12
|
|
|
ENST00000706955.1:c.*772_*773insTCGTACCG
|
ENSP00000516675.1:n.*772_*773insTCGTACCG
|
|
|
ENST00000686459.1:c.*323_*324insTCGTACCG
|
ENSP00000508909.1:n.*323_*324insTCGTACCG
|
|
|
ENST00000688158.1:c.*848_*849insTCGTACCG
|
ENSP00000509254.1:n.*848_*849insTCGTACCG
|
|
|
ENST00000688308.1:c.737_738insTCGTACCG
|
ENSP00000508752.1:p.Leu247ArgfsTer12
|
|
|
ENST00000688922.1:c.658_659insTCGTACCG
|
|
|
|
ENST00000693560.1:c.1256_1257insTCGTACCG
|
ENSP00000509861.1:p.Leu420ArgfsTer12
|
|
|
ENST00000371953.8:c.737_738insTCGTACCG
MANE Select
|
ENSP00000361021.3:p.Leu247ArgfsTer12
|
|
|
ENST00000371953.7:c.737_738insTCGTACCG
|
ENSP00000361021.3:p.Leu247ArgfsTer12
|
|
|
ENST00000472832.2:c.164_165insTCGTACCG
|
ENSP00000483066.1:p.Leu56ArgfsTer12
|
|
|
NM_000314.5:c.737_738insTCGTACCG
|
NP_000305.3:p.Leu247ArgfsTer12
|
|
|
NM_000314.6:c.737_738insTCGTACCG
|
NP_000305.3:p.Leu247ArgfsTer12
|
|
|
NM_001304717.2:c.1256_1257insTCGTACCG
|
NP_001291646.2:p.Leu420ArgfsTer12
|
|
|
NM_001304718.1:c.146_147insTCGTACCG
|
NP_001291647.1:p.Leu50ArgfsTer12
|
|
|
XM_006717926.2:c.692_693insTCGTACCG
|
XP_006717989.1:p.Leu232ArgfsTer12
|
|
|
XM_011539981.1:c.737_738insTCGTACCG
|
XP_011538283.1:p.Leu247ArgfsTer12
|
|
|
XM_011539982.1:c.641_642insTCGTACCG
|
XP_011538284.1:p.Leu215ArgfsTer12
|
|
|
XR_945791.1:n.1307_1308insTCGTACCG
|
|
|
|
NM_000314.7:c.737_738insTCGTACCG
|
NP_000305.3:p.Leu247ArgfsTer12
|
|
|
NM_001304717.5:c.1256_1257insTCGTACCG
|
NP_001291646.4:p.Leu420ArgfsTer12
|
|
|
NM_001304718.2:c.146_147insTCGTACCG
|
NP_001291647.1:p.Leu50ArgfsTer12
|
|
|
NM_000314.8:c.737_738insTCGTACCG
MANE Select
|
NP_000305.3:p.Leu247ArgfsTer12
|
|
