ENST00000377873.8:c.805G=
MANE Select
|
ENSP00000367104.3:p.Glu269=
|
|
ENST00000536626.7:c.388G=
|
ENSP00000442522.1:p.Glu130=
|
|
ENST00000377868.6:c.430G=
|
ENSP00000367099.2:p.Glu144=
|
|
ENST00000377873.7:c.805G=
|
ENSP00000367104.3:p.Glu269=
|
|
ENST00000536626.5:c.388G=
|
ENSP00000442522.1:p.Glu130=
|
|
NM_001161705.1:c.430G=
|
NP_001155177.1:p.Glu144=
|
|
NM_001195.4:c.805G=
|
NP_001186.1:p.Glu269=
|
|
NM_001278606.1:c.388G=
|
NP_001265535.1:p.Glu130=
|
|
NM_001278607.1:c.472G=
|
NP_001265536.1:p.Glu158=
|
|
NM_001278608.1:c.388G=
|
NP_001265537.1:p.Glu130=
|
|
XM_011529312.1:c.388G=
|
XP_011527614.1:p.Glu130=
|
|
XM_017028005.2:c.697G=
|
XP_016883494.1:p.Glu233=
|
|
NM_001195.5:c.805G=
MANE Select
|
NP_001186.1:p.Glu269=
|
|
NM_001161705.2:c.430G=
|
NP_001155177.1:p.Glu144=
|
|
NM_001278606.2:c.388G=
|
NP_001265535.1:p.Glu130=
|
|
NM_001278607.2:c.472G=
|
NP_001265536.1:p.Glu158=
|
|
NM_001278608.2:c.388G=
|
NP_001265537.1:p.Glu130=
|
|