ENST00000697124.1:n.797T>G
|
|
|
ENST00000219596.6:c.1676T>G
MANE Select
|
ENSP00000219596.1:p.Leu559Arg
|
|
ENST00000219596.5:c.1676T>G
|
ENSP00000219596.1:p.Leu559Arg
|
|
ENST00000339854.8:c.1136T>G
|
ENSP00000339639.4:p.Leu379Arg
|
|
ENST00000536379.5:c.1043T>G
|
ENSP00000445079.1:p.Leu348Arg
|
|
ENST00000536980.5:c.1043T>G
|
ENSP00000444178.1:p.Leu348Arg
|
|
ENST00000537682.5:c.1676T>G
|
ENSP00000438611.1:p.Leu559Arg
|
|
ENST00000538326.5:c.*301T>G
|
ENSP00000437486.1:n.*301T>G
|
|
ENST00000539145.5:c.597T>G
|
ENSP00000444471.1:n.597T>G
|
|
ENST00000541159.5:c.1043T>G
|
ENSP00000438711.1:p.Leu348Arg
|
|
ENST00000542898.5:c.1769T>G
|
ENSP00000444615.1:p.Leu590Arg
|
|
ENST00000570511.5:c.1165-631T>G
|
ENSP00000458312.1:n.1165-631T>G
|
|
ENST00000572244.5:c.366T>G
|
ENSP00000461186.1:n.366T>G
|
|
ENST00000574583.5:c.532-631T>G
|
ENSP00000460269.1:n.532-631T>G
|
|
ENST00000576315.5:c.532-237T>G
|
ENSP00000460551.1:n.532-237T>G
|
|
ENST00000621655.1:c.1043T>G
|
ENSP00000481436.1:p.Leu348Arg
|
|
NM_000243.2:c.1676T>G , LRG_190t1:c.1676T>G
|
NP_000234.1:p.Leu559Arg
|
|
NM_001198536.1:c.1043T>G
|
NP_001185465.1:p.Leu348Arg
|
|
XM_017023236.2:c.1673T>G
|
XP_016878725.1:p.Leu558Arg
|
|
XR_001751903.1:n.1865T>G
|
|
|
NM_000243.3:c.1676T>G
MANE Select
|
NP_000234.1:p.Leu559Arg
|
|
NM_001198536.2:c.1043T>G
|
NP_001185465.2:p.Leu348Arg
|
|