ENST00000697124.1:n.1369G>C
|
|
|
ENST00000219596.6:c.2248G>C
MANE Select
|
ENSP00000219596.1:p.Gly750Arg
|
|
ENST00000219596.5:c.2248G>C
|
ENSP00000219596.1:p.Gly750Arg
|
|
ENST00000339854.8:c.1708G>C
|
ENSP00000339639.4:p.Gly570Arg
|
|
ENST00000536379.5:c.1615G>C
|
ENSP00000445079.1:p.Gly539Arg
|
|
ENST00000536980.5:c.*524G>C
|
ENSP00000444178.1:n.*524G>C
|
|
ENST00000537682.5:c.*524G>C
|
ENSP00000438611.1:n.*524G>C
|
|
ENST00000538326.5:c.*873G>C
|
ENSP00000437486.1:n.*873G>C
|
|
ENST00000539145.5:c.1169G>C
|
ENSP00000444471.1:n.1169G>C
|
|
ENST00000541159.5:c.1790G>C
|
ENSP00000438711.1:n.1790G>C
|
|
ENST00000542898.5:c.*524G>C
|
ENSP00000444615.1:n.*524G>C
|
|
ENST00000570511.5:c.1653G>C
|
ENSP00000458312.1:n.1653G>C
|
|
ENST00000572244.5:c.938G>C
|
ENSP00000461186.1:n.938G>C
|
|
ENST00000574583.5:c.1020G>C
|
ENSP00000460269.1:n.1020G>C
|
|
ENST00000576315.5:c.1053G>C
|
ENSP00000460551.1:n.1053G>C
|
|
ENST00000621655.1:c.1785G>C
|
ENSP00000481436.1:n.1785G>C
|
|
NM_000243.2:c.2248G>C , LRG_190t1:c.2248G>C
|
NP_000234.1:p.Gly750Arg
|
|
NM_001198536.1:c.*452G>C
|
NP_001185465.1:n.*452G>C
|
|
XM_017023236.2:c.2245G>C
|
XP_016878725.1:p.Gly749Arg
|
|
NM_000243.3:c.2248G>C
MANE Select
|
NP_000234.1:p.Gly750Arg
|
|
NM_001198536.2:c.*452G>C
|
NP_001185465.2:n.*452G>C
|
|