ENST00000697124.1:n.1225T>A
|
|
|
ENST00000219596.6:c.2104T>A
MANE Select
|
ENSP00000219596.1:p.Ser702Thr
|
|
ENST00000219596.5:c.2104T>A
|
ENSP00000219596.1:p.Ser702Thr
|
|
ENST00000339854.8:c.1564T>A
|
ENSP00000339639.4:p.Ser522Thr
|
|
ENST00000536379.5:c.1471T>A
|
ENSP00000445079.1:p.Ser491Thr
|
|
ENST00000536980.5:c.*380T>A
|
ENSP00000444178.1:n.*380T>A
|
|
ENST00000537682.5:c.*380T>A
|
ENSP00000438611.1:n.*380T>A
|
|
ENST00000538326.5:c.*729T>A
|
ENSP00000437486.1:n.*729T>A
|
|
ENST00000539145.5:c.1025T>A
|
ENSP00000444471.1:n.1025T>A
|
|
ENST00000541159.5:c.1646T>A
|
ENSP00000438711.1:n.1646T>A
|
|
ENST00000542898.5:c.*380T>A
|
ENSP00000444615.1:n.*380T>A
|
|
ENST00000570511.5:c.1509T>A
|
ENSP00000458312.1:n.1509T>A
|
|
ENST00000572244.5:c.794T>A
|
ENSP00000461186.1:n.794T>A
|
|
ENST00000574583.5:c.876T>A
|
ENSP00000460269.1:n.876T>A
|
|
ENST00000576315.5:c.909T>A
|
ENSP00000460551.1:n.909T>A
|
|
ENST00000621655.1:c.1641T>A
|
ENSP00000481436.1:n.1641T>A
|
|
NM_000243.2:c.2104T>A , LRG_190t1:c.2104T>A
|
NP_000234.1:p.Ser702Thr
|
|
NM_001198536.1:c.*308T>A
|
NP_001185465.1:n.*308T>A
|
|
XM_017023236.2:c.2101T>A
|
XP_016878725.1:p.Ser701Thr
|
|
NM_000243.3:c.2104T>A
MANE Select
|
NP_000234.1:p.Ser702Thr
|
|
NM_001198536.2:c.*308T>A
|
NP_001185465.2:n.*308T>A
|
|