ENST00000248633.9:c.2316A=
MANE Select
|
ENSP00000248633.4:p.Val772=
|
|
ENST00000248633.8:c.2316A=
|
ENSP00000248633.4:p.Val772=
|
|
ENST00000428214.5:c.2145A=
|
ENSP00000394413.1:p.Val715=
|
|
ENST00000438045.5:c.1350A=
|
ENSP00000410438.1:p.Val450=
|
|
ENST00000484913.5:n.2355A=
|
|
|
ENST00000496092.1:n.114A=
|
|
|
ENST00000496420.5:n.1992A=
|
|
|
NM_000466.2:c.2316A=
|
NP_000457.1:p.Val772=
|
|
NM_001282677.1:c.2145A=
|
NP_001269606.1:p.Val715=
|
|
NM_001282678.1:c.1692A=
|
NP_001269607.1:p.Val564=
|
|
XM_005250433.3:c.567A=
|
XP_005250490.1:p.Val189=
|
|
XR_242246.3:n.2412A=
|
|
|
XM_017012319.2:c.567A=
|
XP_016867808.1:p.Val189=
|
|
XR_001744808.2:n.1343A=
|
|
|
XR_242246.5:n.2363A=
|
|
|
NM_000466.3:c.2316A=
MANE Select
|
NP_000457.1:p.Val772=
|
|
NM_001282677.2:c.2145A=
|
NP_001269606.1:p.Val715=
|
|
NM_001282678.2:c.1692A=
|
NP_001269607.1:p.Val564=
|
|