|
ENST00000415557.2:c.178G>A
(ACTA2)
|
ENSP00000396730.2:p.Ala60Thr
|
|
|
ENST00000458159.6:c.178G>A
(ACTA2)
|
ENSP00000398239.2:p.Ala60Thr
|
|
|
ENST00000480297.6:n.244G>A
(ACTA2)
|
|
|
|
ENST00000482085.2:n.1659G>A
(ACTA2)
|
|
|
|
ENST00000224784.10:c.178G>A
(ACTA2)
MANE Select
|
ENSP00000224784.6:p.Ala60Thr
|
|
|
ENST00000371927.7:c.1254+24902C>T
(STAMBPL1)
|
ENSP00000360995.3:n.1254+24902C>T
|
|
|
ENST00000415557.1:c.178G>A
(ACTA2)
|
ENSP00000396730.1:p.Ala60Thr
|
|
|
ENST00000458159.5:c.178G>A
(ACTA2)
|
ENSP00000398239.1:p.Ala60Thr
|
|
|
ENST00000458208.5:c.178G>A
(ACTA2)
|
ENSP00000402373.1:p.Ala60Thr
|
|
|
ENST00000480297.5:n.218G>A
(ACTA2)
|
|
|
|
ENST00000488967.5:n.244G>A
(ACTA2)
|
|
|
|
NM_001141945.1:c.178G>A , LRG_781t2:c.178G>A
(ACTA2)
|
NP_001135417.1:p.Ala60Thr
|
|
|
NM_001613.2:c.178G>A , LRG_781t1:c.178G>A
(ACTA2)
|
NP_001604.1:p.Ala60Thr
|
|
|
XM_011540016.1:c.178G>A
(ACTA2)
|
XP_011538318.1:p.Ala60Thr
|
|
|
NM_001141945.2:c.178G>A
(ACTA2)
|
NP_001135417.1:p.Ala60Thr
|
|
|
NM_001320855.1:c.178G>A
(ACTA2)
|
NP_001307784.1:p.Ala60Thr
|
|
|
NM_001613.3:c.178G>A
(ACTA2)
|
NP_001604.1:p.Ala60Thr
|
|
|
NM_001613.4:c.178G>A
(ACTA2)
MANE Select
|
NP_001604.1:p.Ala60Thr
|
|
