ENST00000560563.2:n.742T>G
(ACTC1)
|
|
|
ENST00000290378.6:c.636T>G
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Arg212=
|
|
ENST00000647798.1:n.730T>G
(ACTC1)
|
|
|
ENST00000648556.1:n.793T>G
(ACTC1)
|
|
|
ENST00000650163.1:n.716T>G
(ACTC1)
|
|
|
ENST00000290378.4:c.636T>G
(ACTC1)
|
ENSP00000290378.4:p.Arg212=
|
|
ENST00000557860.1:n.326T>G
(ACTC1)
|
|
|
ENST00000560563.1:n.135T>G
(ACTC1)
|
|
|
NM_005159.4:c.636T>G , LRG_388t1:c.636T>G
(ACTC1)
|
NP_005150.1:p.Arg212=
|
|
NR_120329.1:n.299+14831A>C
(GJD2-DT)
|
|
|
NM_005159.5:c.636T>G
(ACTC1)
MANE Select
|
NP_005150.1:p.Arg212=
|
|