ENST00000218099.7:c.1301_1303delinsAGT
MANE Select
|
ENSP00000218099.2:p.Glu434=
|
|
ENST00000643157.1:n.1723+245_1723+247delinsAGT
|
|
|
ENST00000218099.6:c.1301_1303delinsAGT
|
ENSP00000218099.2:p.Glu434=
|
|
ENST00000394090.2:c.1187_1189delinsAGT
|
ENSP00000377650.2:p.Glu396=
|
|
NM_000133.3:c.1301_1303delinsAGT , LRG_556t1:c.1301_1303delinsAGT
|
NP_000124.1:p.Glu434=
|
|
NM_001313913.1:c.1187_1189delinsAGT
|
NP_001300842.1:p.Glu396=
|
|
XM_005262397.3:c.1172_1174delinsAGT
|
XP_005262454.1:p.Glu391=
|
|
XM_005262397.4:c.1172_1174delinsAGT
|
XP_005262454.1:p.Glu391=
|
|
NM_000133.4:c.1301_1303delinsAGT
MANE Select
|
NP_000124.1:p.Glu434=
|
|
NM_001313913.2:c.1187_1189delinsAGT
|
NP_001300842.1:p.Glu396=
|
|