ENST00000248633.9:c.1534G>T
MANE Select
|
ENSP00000248633.4:p.Asp512Tyr
|
|
ENST00000248633.8:c.1534G>T
|
ENSP00000248633.4:p.Asp512Tyr
|
|
ENST00000422866.1:c.435G>T
|
|
|
ENST00000428214.5:c.1534G>T
|
ENSP00000394413.1:p.Asp512Tyr
|
|
ENST00000438045.5:c.568G>T
|
ENSP00000410438.1:p.Asp190Tyr
|
|
ENST00000476923.1:n.295G>T
|
|
|
ENST00000484913.5:n.1573G>T
|
|
|
NM_000466.2:c.1534G>T
|
NP_000457.1:p.Asp512Tyr
|
|
NM_001282677.1:c.1534G>T
|
NP_001269606.1:p.Asp512Tyr
|
|
NM_001282678.1:c.910G>T
|
NP_001269607.1:p.Asp304Tyr
|
|
XM_005250433.3:c.-133G>T
|
XP_005250490.1:n.-133G>T
|
|
XR_242246.3:n.1630G>T
|
|
|
XM_017012319.2:c.-133G>T
|
XP_016867808.1:n.-133G>T
|
|
XR_001744808.2:n.644G>T
|
|
|
XR_242246.5:n.1581G>T
|
|
|
NM_000466.3:c.1534G>T
MANE Select
|
NP_000457.1:p.Asp512Tyr
|
|
NM_001282677.2:c.1534G>T
|
NP_001269606.1:p.Asp512Tyr
|
|
NM_001282678.2:c.910G>T
|
NP_001269607.1:p.Asp304Tyr
|
|