ENST00000560563.2:n.647G=
(ACTC1)
|
|
|
ENST00000290378.6:c.541G=
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Asp181=
|
|
ENST00000647798.1:n.635G=
(ACTC1)
|
|
|
ENST00000648556.1:n.698G=
(ACTC1)
|
|
|
ENST00000650163.1:n.621G=
(ACTC1)
|
|
|
ENST00000290378.4:c.541G=
(ACTC1)
|
ENSP00000290378.4:p.Asp181=
|
|
ENST00000557860.1:n.231G=
(ACTC1)
|
|
|
ENST00000560563.1:n.40G=
(ACTC1)
|
|
|
NM_005159.4:c.541G= , LRG_388t1:c.541G=
(ACTC1)
|
NP_005150.1:p.Asp181=
|
|
NR_120329.1:n.299+15052C=
(GJD2-DT)
|
|
|
NM_005159.5:c.541G=
(ACTC1)
MANE Select
|
NP_005150.1:p.Asp181=
|
|