ENST00000697124.1:n.1063T>G
|
|
|
ENST00000219596.6:c.1942T>G
MANE Select
|
ENSP00000219596.1:p.Phe648Val
|
|
ENST00000219596.5:c.1942T>G
|
ENSP00000219596.1:p.Phe648Val
|
|
ENST00000339854.8:c.1402T>G
|
ENSP00000339639.4:p.Phe468Val
|
|
ENST00000536379.5:c.1309T>G
|
ENSP00000445079.1:p.Phe437Val
|
|
ENST00000536980.5:c.*218T>G
|
ENSP00000444178.1:n.*218T>G
|
|
ENST00000537682.5:c.*218T>G
|
ENSP00000438611.1:n.*218T>G
|
|
ENST00000538326.5:c.*567T>G
|
ENSP00000437486.1:n.*567T>G
|
|
ENST00000539145.5:c.863T>G
|
ENSP00000444471.1:n.863T>G
|
|
ENST00000541159.5:c.1484T>G
|
ENSP00000438711.1:n.1484T>G
|
|
ENST00000542898.5:c.*218T>G
|
ENSP00000444615.1:n.*218T>G
|
|
ENST00000570511.5:c.1347T>G
|
ENSP00000458312.1:n.1347T>G
|
|
ENST00000572244.5:c.632T>G
|
ENSP00000461186.1:n.632T>G
|
|
ENST00000574583.5:c.714T>G
|
ENSP00000460269.1:n.714T>G
|
|
ENST00000576315.5:c.747T>G
|
ENSP00000460551.1:n.747T>G
|
|
ENST00000621655.1:c.1479T>G
|
ENSP00000481436.1:n.1479T>G
|
|
NM_000243.2:c.1942T>G , LRG_190t1:c.1942T>G
|
NP_000234.1:p.Phe648Val
|
|
NM_001198536.1:c.*146T>G
|
NP_001185465.1:n.*146T>G
|
|
XM_017023236.2:c.1939T>G
|
XP_016878725.1:p.Phe647Val
|
|
NM_000243.3:c.1942T>G
MANE Select
|
NP_000234.1:p.Phe648Val
|
|
NM_001198536.2:c.*146T>G
|
NP_001185465.2:n.*146T>G
|
|