ENST00000697124.1:n.1391G>C
|
|
|
ENST00000219596.6:c.2270G>C
MANE Select
|
ENSP00000219596.1:p.Ser757Thr
|
|
ENST00000219596.5:c.2270G>C
|
ENSP00000219596.1:p.Ser757Thr
|
|
ENST00000339854.8:c.1730G>C
|
ENSP00000339639.4:p.Ser577Thr
|
|
ENST00000536379.5:c.1637G>C
|
ENSP00000445079.1:p.Ser546Thr
|
|
ENST00000536980.5:c.*546G>C
|
ENSP00000444178.1:n.*546G>C
|
|
ENST00000537682.5:c.*546G>C
|
ENSP00000438611.1:n.*546G>C
|
|
ENST00000538326.5:c.*895G>C
|
ENSP00000437486.1:n.*895G>C
|
|
ENST00000539145.5:c.1191G>C
|
ENSP00000444471.1:n.1191G>C
|
|
ENST00000541159.5:c.1812G>C
|
ENSP00000438711.1:n.1812G>C
|
|
ENST00000542898.5:c.*546G>C
|
ENSP00000444615.1:n.*546G>C
|
|
ENST00000570511.5:c.1675G>C
|
ENSP00000458312.1:n.1675G>C
|
|
ENST00000572244.5:c.960G>C
|
ENSP00000461186.1:n.960G>C
|
|
ENST00000574583.5:c.1042G>C
|
ENSP00000460269.1:n.1042G>C
|
|
ENST00000576315.5:c.1075G>C
|
ENSP00000460551.1:n.1075G>C
|
|
ENST00000621655.1:c.1807G>C
|
ENSP00000481436.1:n.1807G>C
|
|
NM_000243.2:c.2270G>C , LRG_190t1:c.2270G>C
|
NP_000234.1:p.Ser757Thr
|
|
NM_001198536.1:c.*474G>C
|
NP_001185465.1:n.*474G>C
|
|
XM_017023236.2:c.2267G>C
|
XP_016878725.1:p.Ser756Thr
|
|
NM_000243.3:c.2270G>C
MANE Select
|
NP_000234.1:p.Ser757Thr
|
|
NM_001198536.2:c.*474G>C
|
NP_001185465.2:n.*474G>C
|
|