ENST00000560563.2:n.671G>T
(ACTC1)
|
|
|
ENST00000290378.6:c.565G>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Asp189Tyr
|
|
ENST00000647798.1:n.659G>T
(ACTC1)
|
|
|
ENST00000648556.1:n.722G>T
(ACTC1)
|
|
|
ENST00000650163.1:n.645G>T
(ACTC1)
|
|
|
ENST00000290378.4:c.565G>T
(ACTC1)
|
ENSP00000290378.4:p.Asp189Tyr
|
|
ENST00000557860.1:n.255G>T
(ACTC1)
|
|
|
ENST00000560563.1:n.64G>T
(ACTC1)
|
|
|
NM_005159.4:c.565G>T , LRG_388t1:c.565G>T
(ACTC1)
|
NP_005150.1:p.Asp189Tyr
|
|
NR_120329.1:n.299+15028C>A
(GJD2-DT)
|
|
|
NM_005159.5:c.565G>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Asp189Tyr
|
|