ENST00000560563.2:n.725G>C
(ACTC1)
|
|
|
ENST00000290378.6:c.619G>C
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Glu207Gln
|
|
ENST00000647798.1:n.713G>C
(ACTC1)
|
|
|
ENST00000648556.1:n.776G>C
(ACTC1)
|
|
|
ENST00000650163.1:n.699G>C
(ACTC1)
|
|
|
ENST00000290378.4:c.619G>C
(ACTC1)
|
ENSP00000290378.4:p.Glu207Gln
|
|
ENST00000557860.1:n.309G>C
(ACTC1)
|
|
|
ENST00000560563.1:n.118G>C
(ACTC1)
|
|
|
NM_005159.4:c.619G>C , LRG_388t1:c.619G>C
(ACTC1)
|
NP_005150.1:p.Glu207Gln
|
|
NR_120329.1:n.299+14848C>G
(GJD2-DT)
|
|
|
NM_005159.5:c.619G>C
(ACTC1)
MANE Select
|
NP_005150.1:p.Glu207Gln
|
|