ENST00000697124.1:n.1439G=
|
|
|
ENST00000219596.6:c.2318G=
MANE Select
|
ENSP00000219596.1:p.Cys773=
|
|
ENST00000219596.5:c.2318G=
|
ENSP00000219596.1:p.Cys773=
|
|
ENST00000339854.8:c.1778G=
|
ENSP00000339639.4:p.Cys593=
|
|
ENST00000536379.5:c.1685G=
|
ENSP00000445079.1:p.Cys562=
|
|
ENST00000536980.5:c.*594G=
|
ENSP00000444178.1:n.*594G=
|
|
ENST00000537682.5:c.*594G=
|
ENSP00000438611.1:n.*594G=
|
|
ENST00000538326.5:c.*943G=
|
ENSP00000437486.1:n.*943G=
|
|
ENST00000539145.5:c.1239G=
|
ENSP00000444471.1:n.1239G=
|
|
ENST00000541159.5:c.1860G=
|
ENSP00000438711.1:n.1860G=
|
|
ENST00000542898.5:c.*594G=
|
ENSP00000444615.1:n.*594G=
|
|
ENST00000570511.5:c.1723G=
|
ENSP00000458312.1:n.1723G=
|
|
ENST00000572244.5:c.1008G=
|
ENSP00000461186.1:n.1008G=
|
|
ENST00000574583.5:c.1090G=
|
ENSP00000460269.1:n.1090G=
|
|
ENST00000576315.5:c.1123G=
|
ENSP00000460551.1:n.1123G=
|
|
ENST00000621655.1:c.1855G=
|
ENSP00000481436.1:n.1855G=
|
|
NM_000243.2:c.2318G= , LRG_190t1:c.2318G=
|
NP_000234.1:p.Cys773=
|
|
NM_001198536.1:c.*522G=
|
NP_001185465.1:n.*522G=
|
|
XM_017023236.2:c.2315G=
|
XP_016878725.1:p.Cys772=
|
|
NM_000243.3:c.2318G=
MANE Select
|
NP_000234.1:p.Cys773=
|
|
NM_001198536.2:c.*522G=
|
NP_001185465.2:n.*522G=
|
|