ENST00000560563.2:n.657G>T
(ACTC1)
|
|
|
ENST00000290378.6:c.551G>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Gly184Val
|
|
ENST00000647798.1:n.645G>T
(ACTC1)
|
|
|
ENST00000648556.1:n.708G>T
(ACTC1)
|
|
|
ENST00000650163.1:n.631G>T
(ACTC1)
|
|
|
ENST00000290378.4:c.551G>T
(ACTC1)
|
ENSP00000290378.4:p.Gly184Val
|
|
ENST00000557860.1:n.241G>T
(ACTC1)
|
|
|
ENST00000560563.1:n.50G>T
(ACTC1)
|
|
|
NM_005159.4:c.551G>T , LRG_388t1:c.551G>T
(ACTC1)
|
NP_005150.1:p.Gly184Val
|
|
NR_120329.1:n.299+15042C>A
(GJD2-DT)
|
|
|
NM_005159.5:c.551G>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Gly184Val
|
|