ENST00000218099.7:c.618A=
MANE Select
|
ENSP00000218099.2:p.Glu206=
|
|
ENST00000643157.1:n.1285A=
|
|
|
ENST00000218099.6:c.618A=
|
ENSP00000218099.2:p.Glu206=
|
|
ENST00000394090.2:c.504A=
|
ENSP00000377650.2:p.Glu168=
|
|
NM_000133.3:c.618A= , LRG_556t1:c.618A=
|
NP_000124.1:p.Glu206=
|
|
NM_001313913.1:c.504A=
|
NP_001300842.1:p.Glu168=
|
|
XM_005262397.3:c.489A=
|
XP_005262454.1:p.Glu163=
|
|
XM_005262397.4:c.489A=
|
XP_005262454.1:p.Glu163=
|
|
NM_000133.4:c.618A=
MANE Select
|
NP_000124.1:p.Glu206=
|
|
NM_001313913.2:c.504A=
|
NP_001300842.1:p.Glu168=
|
|