ENST00000560563.2:n.682G>C
(ACTC1)
|
|
|
ENST00000290378.6:c.576G>C
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Met192Ile
|
|
ENST00000647798.1:n.670G>C
(ACTC1)
|
|
|
ENST00000648556.1:n.733G>C
(ACTC1)
|
|
|
ENST00000650163.1:n.656G>C
(ACTC1)
|
|
|
ENST00000290378.4:c.576G>C
(ACTC1)
|
ENSP00000290378.4:p.Met192Ile
|
|
ENST00000557860.1:n.266G>C
(ACTC1)
|
|
|
ENST00000560563.1:n.75G>C
(ACTC1)
|
|
|
NM_005159.4:c.576G>C , LRG_388t1:c.576G>C
(ACTC1)
|
NP_005150.1:p.Met192Ile
|
|
NR_120329.1:n.299+15017C>G
(GJD2-DT)
|
|
|
NM_005159.5:c.576G>C
(ACTC1)
MANE Select
|
NP_005150.1:p.Met192Ile
|
|