ENST00000248633.9:c.1566G>A
MANE Select
|
ENSP00000248633.4:p.Leu522=
|
|
ENST00000248633.8:c.1566G>A
|
ENSP00000248633.4:p.Leu522=
|
|
ENST00000422866.1:c.467G>A
|
|
|
ENST00000428214.5:c.1566G>A
|
ENSP00000394413.1:p.Leu522=
|
|
ENST00000438045.5:c.600G>A
|
ENSP00000410438.1:p.Leu200=
|
|
ENST00000476923.1:n.327G>A
|
|
|
ENST00000484913.5:n.1605G>A
|
|
|
NM_000466.2:c.1566G>A
|
NP_000457.1:p.Leu522=
|
|
NM_001282677.1:c.1566G>A
|
NP_001269606.1:p.Leu522=
|
|
NM_001282678.1:c.942G>A
|
NP_001269607.1:p.Leu314=
|
|
XM_005250433.3:c.-101G>A
|
XP_005250490.1:n.-101G>A
|
|
XR_242246.3:n.1662G>A
|
|
|
XM_017012319.2:c.-101G>A
|
XP_016867808.1:n.-101G>A
|
|
XR_001744808.2:n.676G>A
|
|
|
XR_242246.5:n.1613G>A
|
|
|
NM_000466.3:c.1566G>A
MANE Select
|
NP_000457.1:p.Leu522=
|
|
NM_001282677.2:c.1566G>A
|
NP_001269606.1:p.Leu522=
|
|
NM_001282678.2:c.942G>A
|
NP_001269607.1:p.Leu314=
|
|