ENST00000560563.2:n.738T>G
(ACTC1)
|
|
|
ENST00000290378.6:c.632T>G
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Val211Gly
|
|
ENST00000647798.1:n.726T>G
(ACTC1)
|
|
|
ENST00000648556.1:n.789T>G
(ACTC1)
|
|
|
ENST00000650163.1:n.712T>G
(ACTC1)
|
|
|
ENST00000290378.4:c.632T>G
(ACTC1)
|
ENSP00000290378.4:p.Val211Gly
|
|
ENST00000557860.1:n.322T>G
(ACTC1)
|
|
|
ENST00000560563.1:n.131T>G
(ACTC1)
|
|
|
NM_005159.4:c.632T>G , LRG_388t1:c.632T>G
(ACTC1)
|
NP_005150.1:p.Val211Gly
|
|
NR_120329.1:n.299+14835A>C
(GJD2-DT)
|
|
|
NM_005159.5:c.632T>G
(ACTC1)
MANE Select
|
NP_005150.1:p.Val211Gly
|
|