ENST00000248633.9:c.2715C>T
MANE Select
|
ENSP00000248633.4:p.Val905=
|
|
ENST00000248633.8:c.2715C>T
|
ENSP00000248633.4:p.Val905=
|
|
ENST00000428214.5:c.2544C>T
|
ENSP00000394413.1:p.Val848=
|
|
ENST00000438045.5:c.1749C>T
|
ENSP00000410438.1:p.Val583=
|
|
ENST00000484913.5:n.2754C>T
|
|
|
ENST00000496420.5:n.2607C>T
|
|
|
NM_000466.2:c.2715C>T
|
NP_000457.1:p.Val905=
|
|
NM_001282677.1:c.2544C>T
|
NP_001269606.1:p.Val848=
|
|
NM_001282678.1:c.2091C>T
|
NP_001269607.1:p.Val697=
|
|
XM_005250433.3:c.966C>T
|
XP_005250490.1:p.Val322=
|
|
XR_242246.3:n.2811C>T
|
|
|
XM_017012319.2:c.966C>T
|
XP_016867808.1:p.Val322=
|
|
XR_001744808.2:n.1742C>T
|
|
|
XR_242246.5:n.2762C>T
|
|
|
NM_000466.3:c.2715C>T
MANE Select
|
NP_000457.1:p.Val905=
|
|
NM_001282677.2:c.2544C>T
|
NP_001269606.1:p.Val848=
|
|
NM_001282678.2:c.2091C>T
|
NP_001269607.1:p.Val697=
|
|