ENST00000560563.2:n.618A>G
(ACTC1)
|
|
|
ENST00000290378.6:c.512A>G
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Tyr171Cys
|
|
ENST00000647798.1:n.606A>G
(ACTC1)
|
|
|
ENST00000648556.1:n.669A>G
(ACTC1)
|
|
|
ENST00000650163.1:n.592A>G
(ACTC1)
|
|
|
ENST00000290378.4:c.512A>G
(ACTC1)
|
ENSP00000290378.4:p.Tyr171Cys
|
|
ENST00000557860.1:n.202A>G
(ACTC1)
|
|
|
ENST00000560563.1:n.11A>G
(ACTC1)
|
|
|
NM_005159.4:c.512A>G , LRG_388t1:c.512A>G
(ACTC1)
|
NP_005150.1:p.Tyr171Cys
|
|
NR_120329.1:n.299+15081T>C
(GJD2-DT)
|
|
|
NM_005159.5:c.512A>G
(ACTC1)
MANE Select
|
NP_005150.1:p.Tyr171Cys
|
|