ENST00000560563.2:n.632G>T
(ACTC1)
|
|
|
ENST00000290378.6:c.526G>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Ala176Ser
|
|
ENST00000647798.1:n.620G>T
(ACTC1)
|
|
|
ENST00000648556.1:n.683G>T
(ACTC1)
|
|
|
ENST00000650163.1:n.606G>T
(ACTC1)
|
|
|
ENST00000290378.4:c.526G>T
(ACTC1)
|
ENSP00000290378.4:p.Ala176Ser
|
|
ENST00000557860.1:n.216G>T
(ACTC1)
|
|
|
ENST00000560563.1:n.25G>T
(ACTC1)
|
|
|
NM_005159.4:c.526G>T , LRG_388t1:c.526G>T
(ACTC1)
|
NP_005150.1:p.Ala176Ser
|
|
NR_120329.1:n.299+15067C>A
(GJD2-DT)
|
|
|
NM_005159.5:c.526G>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Ala176Ser
|
|