ENST00000248633.9:c.2713G=
MANE Select
|
ENSP00000248633.4:p.Val905=
|
|
ENST00000248633.8:c.2713G=
|
ENSP00000248633.4:p.Val905=
|
|
ENST00000428214.5:c.2542G=
|
ENSP00000394413.1:p.Val848=
|
|
ENST00000438045.5:c.1747G=
|
ENSP00000410438.1:p.Val583=
|
|
ENST00000484913.5:n.2752G=
|
|
|
ENST00000496420.5:n.2605G=
|
|
|
NM_000466.2:c.2713G=
|
NP_000457.1:p.Val905=
|
|
NM_001282677.1:c.2542G=
|
NP_001269606.1:p.Val848=
|
|
NM_001282678.1:c.2089G=
|
NP_001269607.1:p.Val697=
|
|
XM_005250433.3:c.964G=
|
XP_005250490.1:p.Val322=
|
|
XR_242246.3:n.2809G=
|
|
|
XM_017012319.2:c.964G=
|
XP_016867808.1:p.Val322=
|
|
XR_001744808.2:n.1740G=
|
|
|
XR_242246.5:n.2760G=
|
|
|
NM_000466.3:c.2713G=
MANE Select
|
NP_000457.1:p.Val905=
|
|
NM_001282677.2:c.2542G=
|
NP_001269606.1:p.Val848=
|
|
NM_001282678.2:c.2089G=
|
NP_001269607.1:p.Val697=
|
|