ENST00000697291.1:c.*872A=
|
ENSP00000513228.1:n.*872A=
|
|
ENST00000648433.1:c.1275A=
|
ENSP00000496816.1:p.Glu425=
|
|
ENST00000649554.1:n.885A=
|
|
|
ENST00000649979.2:c.1275A=
MANE Select
|
ENSP00000497271.1:p.Glu425=
|
|
ENST00000679938.1:c.963A=
|
ENSP00000505518.1:p.Glu321=
|
|
ENST00000263642.2:c.1275A=
|
ENSP00000263642.2:p.Glu425=
|
|
NM_022168.3:c.1275A=
|
NP_071451.2:p.Glu425=
|
|
XM_011511628.1:c.558A=
|
XP_011509930.1:p.Glu186=
|
|
XM_011511629.1:c.1275A=
|
XP_011509931.1:p.Glu425=
|
|
NM_022168.4:c.1275A=
MANE Select
|
NP_071451.2:p.Glu425=
|
|