ENST00000248633.9:c.916T>G
MANE Select
|
ENSP00000248633.4:p.Phe306Val
|
|
ENST00000248633.8:c.916T>G
|
ENSP00000248633.4:p.Phe306Val
|
|
ENST00000428214.5:c.916T>G
|
ENSP00000394413.1:p.Phe306Val
|
|
ENST00000438045.5:c.274-3632T>G
|
ENSP00000410438.1:n.274-3632T>G
|
|
ENST00000484913.5:n.955T>G
|
|
|
NM_000466.2:c.916T>G
|
NP_000457.1:p.Phe306Val
|
|
NM_001282677.1:c.916T>G
|
NP_001269606.1:p.Phe306Val
|
|
NM_001282678.1:c.292T>G
|
NP_001269607.1:p.Phe98Val
|
|
XR_242246.3:n.1012T>G
|
|
|
XM_017012319.2:c.-751T>G
|
XP_016867808.1:n.-751T>G
|
|
XR_001744808.2:n.26T>G
|
|
|
XR_242246.5:n.963T>G
|
|
|
NM_000466.3:c.916T>G
MANE Select
|
NP_000457.1:p.Phe306Val
|
|
NM_001282677.2:c.916T>G
|
NP_001269606.1:p.Phe306Val
|
|
NM_001282678.2:c.292T>G
|
NP_001269607.1:p.Phe98Val
|
|