ENST00000697124.1:n.1304G>C
|
|
|
ENST00000219596.6:c.2183G>C
MANE Select
|
ENSP00000219596.1:p.Ser728Thr
|
|
ENST00000219596.5:c.2183G>C
|
ENSP00000219596.1:p.Ser728Thr
|
|
ENST00000339854.8:c.1643G>C
|
ENSP00000339639.4:p.Ser548Thr
|
|
ENST00000536379.5:c.1550G>C
|
ENSP00000445079.1:p.Ser517Thr
|
|
ENST00000536980.5:c.*459G>C
|
ENSP00000444178.1:n.*459G>C
|
|
ENST00000537682.5:c.*459G>C
|
ENSP00000438611.1:n.*459G>C
|
|
ENST00000538326.5:c.*808G>C
|
ENSP00000437486.1:n.*808G>C
|
|
ENST00000539145.5:c.1104G>C
|
ENSP00000444471.1:n.1104G>C
|
|
ENST00000541159.5:c.1725G>C
|
ENSP00000438711.1:n.1725G>C
|
|
ENST00000542898.5:c.*459G>C
|
ENSP00000444615.1:n.*459G>C
|
|
ENST00000570511.5:c.1588G>C
|
ENSP00000458312.1:n.1588G>C
|
|
ENST00000572244.5:c.873G>C
|
ENSP00000461186.1:n.873G>C
|
|
ENST00000574583.5:c.955G>C
|
ENSP00000460269.1:n.955G>C
|
|
ENST00000576315.5:c.988G>C
|
ENSP00000460551.1:n.988G>C
|
|
ENST00000621655.1:c.1720G>C
|
ENSP00000481436.1:n.1720G>C
|
|
NM_000243.2:c.2183G>C , LRG_190t1:c.2183G>C
|
NP_000234.1:p.Ser728Thr
|
|
NM_001198536.1:c.*387G>C
|
NP_001185465.1:n.*387G>C
|
|
XM_017023236.2:c.2180G>C
|
XP_016878725.1:p.Ser727Thr
|
|
NM_000243.3:c.2183G>C
MANE Select
|
NP_000234.1:p.Ser728Thr
|
|
NM_001198536.2:c.*387G>C
|
NP_001185465.2:n.*387G>C
|
|