ENST00000373113.8:c.646G=
MANE Select
|
ENSP00000362205.3:p.Asp216=
|
|
ENST00000338469.3:c.483-123G=
|
ENSP00000342651.4:n.483-123G=
|
|
ENST00000373113.7:c.646G=
|
ENSP00000362205.3:p.Asp216=
|
|
ENST00000373122.8:c.*17G=
|
ENSP00000362214.4:n.*17G=
|
|
NM_001271821.1:c.483-123G=
|
NP_001258750.1:n.483-123G=
|
|
NM_018965.3:c.646G= , LRG_631t1:c.646G=
|
NP_061838.1:p.Asp216=
|
|
XM_006715116.2:c.385G=
|
XP_006715179.1:p.Asp129=
|
|
XR_926795.1:n.222+3340C=
|
|
|
XR_926796.1:n.214+3340C=
|
|
|
XR_926797.1:n.188+3340C=
|
|
|
XR_926795.2:n.517+3340C=
|
|
|
XR_926797.2:n.232+3340C=
|
|
|
NM_001271821.2:c.483-123G=
|
NP_001258750.1:n.483-123G=
|
|
NM_018965.4:c.646G=
MANE Select
|
NP_061838.1:p.Asp216=
|
|