ENST00000248633.9:c.503G>C
MANE Select
|
ENSP00000248633.4:p.Arg168Thr
|
|
ENST00000248633.8:c.503G>C
|
ENSP00000248633.4:p.Arg168Thr
|
|
ENST00000428214.5:c.503G>C
|
ENSP00000394413.1:p.Arg168Thr
|
|
ENST00000438045.5:c.274-4045G>C
|
ENSP00000410438.1:n.274-4045G>C
|
|
ENST00000484913.5:n.542G>C
|
|
|
NM_000466.2:c.503G>C
|
NP_000457.1:p.Arg168Thr
|
|
NM_001282677.1:c.503G>C
|
NP_001269606.1:p.Arg168Thr
|
|
NM_001282678.1:c.-122G>C
|
NP_001269607.1:n.-122G>C
|
|
XR_242246.3:n.599G>C
|
|
|
XR_242246.5:n.550G>C
|
|
|
NM_000466.3:c.503G>C
MANE Select
|
NP_000457.1:p.Arg168Thr
|
|
NM_001282677.2:c.503G>C
|
NP_001269606.1:p.Arg168Thr
|
|
NM_001282678.2:c.-122G>C
|
NP_001269607.1:n.-122G>C
|
|