ENST00000560563.2:n.660G=
(ACTC1)
|
|
|
ENST00000290378.6:c.554G=
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Arg185=
|
|
ENST00000647798.1:n.648G=
(ACTC1)
|
|
|
ENST00000648556.1:n.711G=
(ACTC1)
|
|
|
ENST00000650163.1:n.634G=
(ACTC1)
|
|
|
ENST00000290378.4:c.554G=
(ACTC1)
|
ENSP00000290378.4:p.Arg185=
|
|
ENST00000557860.1:n.244G=
(ACTC1)
|
|
|
ENST00000560563.1:n.53G=
(ACTC1)
|
|
|
NM_005159.4:c.554G= , LRG_388t1:c.554G=
(ACTC1)
|
NP_005150.1:p.Arg185=
|
|
NR_120329.1:n.299+15039C=
(GJD2-DT)
|
|
|
NM_005159.5:c.554G=
(ACTC1)
MANE Select
|
NP_005150.1:p.Arg185=
|
|