ENST00000292180.8:c.1594C>T
MANE Select
|
ENSP00000292180.3:p.Leu532=
|
|
ENST00000292180.7:c.1594C>T
|
ENSP00000292180.3:p.Leu532=
|
|
ENST00000295530.6:c.*11+79C>T
|
ENSP00000295530.2:n.*11+79C>T
|
|
ENST00000315144.14:c.1303C>T
|
ENSP00000317296.10:p.Leu435=
|
|
ENST00000368428.1:c.217C>T
|
ENSP00000357413.1:p.Leu73=
|
|
ENST00000368432.5:c.1303C>T
|
ENSP00000357417.1:p.Leu435=
|
|
ENST00000477609.5:n.344+79C>T
|
|
|
ENST00000481758.1:n.164C>T
|
|
|
ENST00000489992.5:n.404C>T
|
|
|
NM_001184891.1:c.1303C>T
|
NP_001171820.1:p.Leu435=
|
|
NM_025207.4:c.1594C>T
|
NP_079483.3:p.Leu532=
|
|
NM_201398.2:c.1303C>T
|
NP_958800.1:p.Leu435=
|
|
XM_005245503.2:c.793C>T
|
XP_005245560.1:p.Leu265=
|
|
XR_241098.3:n.1364C>T
|
|
|
NM_025207.5:c.1594C>T
MANE Select
|
NP_079483.3:p.Leu532=
|
|
NM_001184891.2:c.1303C>T
|
NP_001171820.1:p.Leu435=
|
|
NM_201398.3:c.1303C>T
|
NP_958800.1:p.Leu435=
|
|