ENST00000697124.1:n.1388T>G
|
|
|
ENST00000219596.6:c.2267T>G
MANE Select
|
ENSP00000219596.1:p.Phe756Cys
|
|
ENST00000219596.5:c.2267T>G
|
ENSP00000219596.1:p.Phe756Cys
|
|
ENST00000339854.8:c.1727T>G
|
ENSP00000339639.4:p.Phe576Cys
|
|
ENST00000536379.5:c.1634T>G
|
ENSP00000445079.1:p.Phe545Cys
|
|
ENST00000536980.5:c.*543T>G
|
ENSP00000444178.1:n.*543T>G
|
|
ENST00000537682.5:c.*543T>G
|
ENSP00000438611.1:n.*543T>G
|
|
ENST00000538326.5:c.*892T>G
|
ENSP00000437486.1:n.*892T>G
|
|
ENST00000539145.5:c.1188T>G
|
ENSP00000444471.1:n.1188T>G
|
|
ENST00000541159.5:c.1809T>G
|
ENSP00000438711.1:n.1809T>G
|
|
ENST00000542898.5:c.*543T>G
|
ENSP00000444615.1:n.*543T>G
|
|
ENST00000570511.5:c.1672T>G
|
ENSP00000458312.1:n.1672T>G
|
|
ENST00000572244.5:c.957T>G
|
ENSP00000461186.1:n.957T>G
|
|
ENST00000574583.5:c.1039T>G
|
ENSP00000460269.1:n.1039T>G
|
|
ENST00000576315.5:c.1072T>G
|
ENSP00000460551.1:n.1072T>G
|
|
ENST00000621655.1:c.1804T>G
|
ENSP00000481436.1:n.1804T>G
|
|
NM_000243.2:c.2267T>G , LRG_190t1:c.2267T>G
|
NP_000234.1:p.Phe756Cys
|
|
NM_001198536.1:c.*471T>G
|
NP_001185465.1:n.*471T>G
|
|
XM_017023236.2:c.2264T>G
|
XP_016878725.1:p.Phe755Cys
|
|
NM_000243.3:c.2267T>G
MANE Select
|
NP_000234.1:p.Phe756Cys
|
|
NM_001198536.2:c.*471T>G
|
NP_001185465.2:n.*471T>G
|
|