ENST00000375128.5:c.750_752dup
MANE Select
|
ENSP00000364270.5:p.Glu250_Asn251insLys
|
|
ENST00000375128.4:c.750_752dup
|
ENSP00000364270.4:p.Glu250_Asn251insLys
|
|
ENST00000462523.5:c.*186_*188dup
|
ENSP00000433006.1:n.*186_*188dup
|
|
ENST00000485042.1:n.262_264dup
|
|
|
NM_000380.3:c.750_752dup , LRG_471t1:c.750_752dup
|
NP_000371.1:p.Glu250_Asn251insLys
|
|
NR_027302.1:n.1098_1100dup
|
|
|
XM_006717278.1:c.750_752dup
|
XP_006717341.1:p.Glu250_Asn251insLys
|
|
XM_011518988.1:c.750_752dup
|
XP_011517290.1:p.Glu250_Asn251insLys
|
|
XR_929839.1:n.1281_1283dup
|
|
|
NM_001354975.1:c.624_626dup
|
NP_001341904.1:p.Glu208_Asn209insLys
|
|
NR_149091.1:n.595_597dup
|
|
|
NR_149092.1:n.761_763dup
|
|
|
NR_149093.1:n.1287_1289dup
|
|
|
NR_149094.1:n.1181_1183dup
|
|
|
NM_000380.4:c.750_752dup
MANE Select
|
NP_000371.1:p.Glu250_Asn251insLys
|
|
NM_001354975.2:c.624_626dup
|
NP_001341904.1:p.Glu208_Asn209insLys
|
|
NR_027302.2:n.1029_1031dup
|
|
|
NR_149091.2:n.526_528dup
|
|
|
NR_149092.2:n.692_694dup
|
|
|
NR_149093.2:n.1218_1220dup
|
|
|
NR_149094.2:n.1112_1114dup
|
|
|