ENST00000560563.2:n.650C>G
(ACTC1)
|
|
|
ENST00000290378.6:c.544C>G
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Leu182Val
|
|
ENST00000647798.1:n.638C>G
(ACTC1)
|
|
|
ENST00000648556.1:n.701C>G
(ACTC1)
|
|
|
ENST00000650163.1:n.624C>G
(ACTC1)
|
|
|
ENST00000290378.4:c.544C>G
(ACTC1)
|
ENSP00000290378.4:p.Leu182Val
|
|
ENST00000557860.1:n.234C>G
(ACTC1)
|
|
|
ENST00000560563.1:n.43C>G
(ACTC1)
|
|
|
NM_005159.4:c.544C>G , LRG_388t1:c.544C>G
(ACTC1)
|
NP_005150.1:p.Leu182Val
|
|
NR_120329.1:n.299+15049G>C
(GJD2-DT)
|
|
|
NM_005159.5:c.544C>G
(ACTC1)
MANE Select
|
NP_005150.1:p.Leu182Val
|
|