|
ENST00000415557.2:c.231C>T
(ACTA2)
|
ENSP00000396730.2:p.Ile77=
|
|
|
ENST00000458159.6:c.231C>T
(ACTA2)
|
ENSP00000398239.2:p.Ile77=
|
|
|
ENST00000480297.6:n.297C>T
(ACTA2)
|
|
|
|
ENST00000482085.2:n.1712C>T
(ACTA2)
|
|
|
|
ENST00000224784.10:c.231C>T
(ACTA2)
MANE Select
|
ENSP00000224784.6:p.Ile77=
|
|
|
ENST00000371927.7:c.1254+24849G>A
(STAMBPL1)
|
ENSP00000360995.3:n.1254+24849G>A
|
|
|
ENST00000415557.1:c.231C>T
(ACTA2)
|
ENSP00000396730.1:p.Ile77=
|
|
|
ENST00000458159.5:c.231C>T
(ACTA2)
|
ENSP00000398239.1:p.Ile77=
|
|
|
ENST00000458208.5:c.231C>T
(ACTA2)
|
ENSP00000402373.1:p.Ile77=
|
|
|
ENST00000480297.5:n.271C>T
(ACTA2)
|
|
|
|
ENST00000488967.5:n.297C>T
(ACTA2)
|
|
|
|
NM_001141945.1:c.231C>T , LRG_781t2:c.231C>T
(ACTA2)
|
NP_001135417.1:p.Ile77=
|
|
|
NM_001613.2:c.231C>T , LRG_781t1:c.231C>T
(ACTA2)
|
NP_001604.1:p.Ile77=
|
|
|
XM_011540016.1:c.231C>T
(ACTA2)
|
XP_011538318.1:p.Ile77=
|
|
|
NM_001141945.2:c.231C>T
(ACTA2)
|
NP_001135417.1:p.Ile77=
|
|
|
NM_001320855.1:c.231C>T
(ACTA2)
|
NP_001307784.1:p.Ile77=
|
|
|
NM_001613.3:c.231C>T
(ACTA2)
|
NP_001604.1:p.Ile77=
|
|
|
NM_001613.4:c.231C>T
(ACTA2)
MANE Select
|
NP_001604.1:p.Ile77=
|
|
