ENST00000248633.9:c.2405C>A
MANE Select
|
ENSP00000248633.4:p.Ser802Tyr
|
|
ENST00000248633.8:c.2405C>A
|
ENSP00000248633.4:p.Ser802Tyr
|
|
ENST00000428214.5:c.2234C>A
|
ENSP00000394413.1:p.Ser745Tyr
|
|
ENST00000438045.5:c.1439C>A
|
ENSP00000410438.1:p.Ser480Tyr
|
|
ENST00000484913.5:n.2444C>A
|
|
|
ENST00000496092.1:n.203C>A
|
|
|
ENST00000496420.5:n.2081C>A
|
|
|
NM_000466.2:c.2405C>A
|
NP_000457.1:p.Ser802Tyr
|
|
NM_001282677.1:c.2234C>A
|
NP_001269606.1:p.Ser745Tyr
|
|
NM_001282678.1:c.1781C>A
|
NP_001269607.1:p.Ser594Tyr
|
|
XM_005250433.3:c.656C>A
|
XP_005250490.1:p.Ser219Tyr
|
|
XR_242246.3:n.2501C>A
|
|
|
XM_017012319.2:c.656C>A
|
XP_016867808.1:p.Ser219Tyr
|
|
XR_001744808.2:n.1432C>A
|
|
|
XR_242246.5:n.2452C>A
|
|
|
NM_000466.3:c.2405C>A
MANE Select
|
NP_000457.1:p.Ser802Tyr
|
|
NM_001282677.2:c.2234C>A
|
NP_001269606.1:p.Ser745Tyr
|
|
NM_001282678.2:c.1781C>A
|
NP_001269607.1:p.Ser594Tyr
|
|