ENST00000560563.2:n.740C>A
(ACTC1)
|
|
|
ENST00000290378.6:c.634C>A
(ACTC1)
MANE Select
|
ENSP00000290378.4:p.Arg212Ser
|
|
ENST00000647798.1:n.728C>A
(ACTC1)
|
|
|
ENST00000648556.1:n.791C>A
(ACTC1)
|
|
|
ENST00000650163.1:n.714C>A
(ACTC1)
|
|
|
ENST00000290378.4:c.634C>A
(ACTC1)
|
ENSP00000290378.4:p.Arg212Ser
|
|
ENST00000557860.1:n.324C>A
(ACTC1)
|
|
|
ENST00000560563.1:n.133C>A
(ACTC1)
|
|
|
NM_005159.4:c.634C>A , LRG_388t1:c.634C>A
(ACTC1)
|
NP_005150.1:p.Arg212Ser
|
|
NR_120329.1:n.299+14833G>T
(GJD2-DT)
|
|
|
NM_005159.5:c.634C>A
(ACTC1)
MANE Select
|
NP_005150.1:p.Arg212Ser
|
|