ENST00000560563.2:n.611G>A
(ACTC1)
|
|
|
ENST00000290378.6:c.505G>A
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Glu169Lys
|
|
ENST00000647798.1:n.599G>A
(ACTC1)
|
|
|
ENST00000648556.1:n.662G>A
(ACTC1)
|
|
|
ENST00000650163.1:n.585G>A
(ACTC1)
|
|
|
ENST00000290378.4:c.505G>A
(ACTC1)
|
ENSP00000290378.4:p.Glu169Lys
|
|
ENST00000557860.1:n.195G>A
(ACTC1)
|
|
|
ENST00000560563.1:n.4G>A
(ACTC1)
|
|
|
NM_005159.4:c.505G>A , LRG_388t1:c.505G>A
(ACTC1)
|
NP_005150.1:p.Glu169Lys
|
|
NR_120329.1:n.299+15088C>T
(GJD2-DT)
|
|
|
NM_005159.5:c.505G>A
(ACTC1)
MANE Select
|
NP_005150.1:p.Glu169Lys
|
|