ENST00000560563.2:n.610T>C
(ACTC1)
|
|
|
ENST00000290378.6:c.504T>C
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Tyr168=
|
|
ENST00000647798.1:n.598T>C
(ACTC1)
|
|
|
ENST00000648556.1:n.661T>C
(ACTC1)
|
|
|
ENST00000650163.1:n.584T>C
(ACTC1)
|
|
|
ENST00000290378.4:c.504T>C
(ACTC1)
|
ENSP00000290378.4:p.Tyr168=
|
|
ENST00000557860.1:n.194T>C
(ACTC1)
|
|
|
ENST00000560563.1:n.3T>C
(ACTC1)
|
|
|
NM_005159.4:c.504T>C , LRG_388t1:c.504T>C
(ACTC1)
|
NP_005150.1:p.Tyr168=
|
|
NR_120329.1:n.299+15089A>G
(GJD2-DT)
|
|
|
NM_005159.5:c.504T>C
(ACTC1)
MANE Select
|
NP_005150.1:p.Tyr168=
|
|