ENST00000248633.9:c.917T>C
MANE Select
|
ENSP00000248633.4:p.Phe306Ser
|
|
ENST00000248633.8:c.917T>C
|
ENSP00000248633.4:p.Phe306Ser
|
|
ENST00000428214.5:c.917T>C
|
ENSP00000394413.1:p.Phe306Ser
|
|
ENST00000438045.5:c.274-3631T>C
|
ENSP00000410438.1:n.274-3631T>C
|
|
ENST00000484913.5:n.956T>C
|
|
|
NM_000466.2:c.917T>C
|
NP_000457.1:p.Phe306Ser
|
|
NM_001282677.1:c.917T>C
|
NP_001269606.1:p.Phe306Ser
|
|
NM_001282678.1:c.293T>C
|
NP_001269607.1:p.Phe98Ser
|
|
XR_242246.3:n.1013T>C
|
|
|
XM_017012319.2:c.-750T>C
|
XP_016867808.1:n.-750T>C
|
|
XR_001744808.2:n.27T>C
|
|
|
XR_242246.5:n.964T>C
|
|
|
NM_000466.3:c.917T>C
MANE Select
|
NP_000457.1:p.Phe306Ser
|
|
NM_001282677.2:c.917T>C
|
NP_001269606.1:p.Phe306Ser
|
|
NM_001282678.2:c.293T>C
|
NP_001269607.1:p.Phe98Ser
|
|