ENST00000248633.9:c.2031G>T
MANE Select
|
ENSP00000248633.4:p.Glu677Asp
|
|
ENST00000248633.8:c.2031G>T
|
ENSP00000248633.4:p.Glu677Asp
|
|
ENST00000428214.5:c.1900+1476G>T
|
ENSP00000394413.1:n.1900+1476G>T
|
|
ENST00000438045.5:c.1065G>T
|
ENSP00000410438.1:p.Glu355Asp
|
|
ENST00000484913.5:n.2070G>T
|
|
|
ENST00000496420.5:n.1707G>T
|
|
|
NM_000466.2:c.2031G>T
|
NP_000457.1:p.Glu677Asp
|
|
NM_001282677.1:c.1900+1476G>T
|
NP_001269606.1:n.1900+1476G>T
|
|
NM_001282678.1:c.1407G>T
|
NP_001269607.1:p.Glu469Asp
|
|
XM_005250433.3:c.282G>T
|
XP_005250490.1:p.Glu94Asp
|
|
XR_242246.3:n.2127G>T
|
|
|
XM_017012319.2:c.282G>T
|
XP_016867808.1:p.Glu94Asp
|
|
XR_001744808.2:n.1058G>T
|
|
|
XR_242246.5:n.2078G>T
|
|
|
NM_000466.3:c.2031G>T
MANE Select
|
NP_000457.1:p.Glu677Asp
|
|
NM_001282677.2:c.1900+1476G>T
|
NP_001269606.1:n.1900+1476G>T
|
|
NM_001282678.2:c.1407G>T
|
NP_001269607.1:p.Glu469Asp
|
|