ENST00000560563.2:n.723C>T
(ACTC1)
|
|
|
ENST00000290378.6:c.617C>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Ala206Val
|
|
ENST00000647798.1:n.711C>T
(ACTC1)
|
|
|
ENST00000648556.1:n.774C>T
(ACTC1)
|
|
|
ENST00000650163.1:n.697C>T
(ACTC1)
|
|
|
ENST00000290378.4:c.617C>T
(ACTC1)
|
ENSP00000290378.4:p.Ala206Val
|
|
ENST00000557860.1:n.307C>T
(ACTC1)
|
|
|
ENST00000560563.1:n.116C>T
(ACTC1)
|
|
|
NM_005159.4:c.617C>T , LRG_388t1:c.617C>T
(ACTC1)
|
NP_005150.1:p.Ala206Val
|
|
NR_120329.1:n.299+14850G>A
(GJD2-DT)
|
|
|
NM_005159.5:c.617C>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Ala206Val
|
|