ENST00000697124.1:n.1260G>T
|
|
|
ENST00000219596.6:c.2139G>T
MANE Select
|
ENSP00000219596.1:p.Glu713Asp
|
|
ENST00000219596.5:c.2139G>T
|
ENSP00000219596.1:p.Glu713Asp
|
|
ENST00000339854.8:c.1599G>T
|
ENSP00000339639.4:p.Glu533Asp
|
|
ENST00000536379.5:c.1506G>T
|
ENSP00000445079.1:p.Glu502Asp
|
|
ENST00000536980.5:c.*415G>T
|
ENSP00000444178.1:n.*415G>T
|
|
ENST00000537682.5:c.*415G>T
|
ENSP00000438611.1:n.*415G>T
|
|
ENST00000538326.5:c.*764G>T
|
ENSP00000437486.1:n.*764G>T
|
|
ENST00000539145.5:c.1060G>T
|
ENSP00000444471.1:n.1060G>T
|
|
ENST00000541159.5:c.1681G>T
|
ENSP00000438711.1:n.1681G>T
|
|
ENST00000542898.5:c.*415G>T
|
ENSP00000444615.1:n.*415G>T
|
|
ENST00000570511.5:c.1544G>T
|
ENSP00000458312.1:n.1544G>T
|
|
ENST00000572244.5:c.829G>T
|
ENSP00000461186.1:n.829G>T
|
|
ENST00000574583.5:c.911G>T
|
ENSP00000460269.1:n.911G>T
|
|
ENST00000576315.5:c.944G>T
|
ENSP00000460551.1:n.944G>T
|
|
ENST00000621655.1:c.1676G>T
|
ENSP00000481436.1:n.1676G>T
|
|
NM_000243.2:c.2139G>T , LRG_190t1:c.2139G>T
|
NP_000234.1:p.Glu713Asp
|
|
NM_001198536.1:c.*343G>T
|
NP_001185465.1:n.*343G>T
|
|
XM_017023236.2:c.2136G>T
|
XP_016878725.1:p.Glu712Asp
|
|
NM_000243.3:c.2139G>T
MANE Select
|
NP_000234.1:p.Glu713Asp
|
|
NM_001198536.2:c.*343G>T
|
NP_001185465.2:n.*343G>T
|
|