ENST00000560563.2:n.633C>T
(ACTC1)
|
|
|
ENST00000290378.6:c.527C>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Ala176Val
|
|
ENST00000647798.1:n.621C>T
(ACTC1)
|
|
|
ENST00000648556.1:n.684C>T
(ACTC1)
|
|
|
ENST00000650163.1:n.607C>T
(ACTC1)
|
|
|
ENST00000290378.4:c.527C>T
(ACTC1)
|
ENSP00000290378.4:p.Ala176Val
|
|
ENST00000557860.1:n.217C>T
(ACTC1)
|
|
|
ENST00000560563.1:n.26C>T
(ACTC1)
|
|
|
NM_005159.4:c.527C>T , LRG_388t1:c.527C>T
(ACTC1)
|
NP_005150.1:p.Ala176Val
|
|
NR_120329.1:n.299+15066G>A
(GJD2-DT)
|
|
|
NM_005159.5:c.527C>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Ala176Val
|
|