ENST00000560563.2:n.744A>G
(ACTC1)
|
|
|
ENST00000290378.6:c.638A>G
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Asp213Gly
|
|
ENST00000647798.1:n.732A>G
(ACTC1)
|
|
|
ENST00000648556.1:n.795A>G
(ACTC1)
|
|
|
ENST00000650163.1:n.718A>G
(ACTC1)
|
|
|
ENST00000290378.4:c.638A>G
(ACTC1)
|
ENSP00000290378.4:p.Asp213Gly
|
|
ENST00000557860.1:n.328A>G
(ACTC1)
|
|
|
ENST00000560563.1:n.137A>G
(ACTC1)
|
|
|
NM_005159.4:c.638A>G , LRG_388t1:c.638A>G
(ACTC1)
|
NP_005150.1:p.Asp213Gly
|
|
NR_120329.1:n.299+14829T>C
(GJD2-DT)
|
|
|
NM_005159.5:c.638A>G
(ACTC1)
MANE Select
|
NP_005150.1:p.Asp213Gly
|
|