ENST00000560563.2:n.703C>T
(ACTC1)
|
|
|
ENST00000290378.6:c.597C>T
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Gly199=
|
|
ENST00000647798.1:n.691C>T
(ACTC1)
|
|
|
ENST00000648556.1:n.754C>T
(ACTC1)
|
|
|
ENST00000650163.1:n.677C>T
(ACTC1)
|
|
|
ENST00000290378.4:c.597C>T
(ACTC1)
|
ENSP00000290378.4:p.Gly199=
|
|
ENST00000557860.1:n.287C>T
(ACTC1)
|
|
|
ENST00000560563.1:n.96C>T
(ACTC1)
|
|
|
NM_005159.4:c.597C>T , LRG_388t1:c.597C>T
(ACTC1)
|
NP_005150.1:p.Gly199=
|
|
NR_120329.1:n.299+14996G>A
(GJD2-DT)
|
|
|
NM_005159.5:c.597C>T
(ACTC1)
MANE Select
|
NP_005150.1:p.Gly199=
|
|