ENST00000588860.6:c.1186G>T
|
ENSP00000465878.2:p.Asp396Tyr
|
|
ENST00000589076.6:c.1186G>T
|
ENSP00000466934.2:p.Asp396Tyr
|
|
ENST00000589941.2:c.1186G>T
|
ENSP00000465874.2:p.Asp396Tyr
|
|
ENST00000590061.2:c.1186G>T
|
ENSP00000464772.2:p.Asp396Tyr
|
|
ENST00000593223.2:c.1186G>T
|
ENSP00000466118.2:p.Asp396Tyr
|
|
ENST00000611848.2:c.1186G>T
|
ENSP00000478613.2:p.Asp396Tyr
|
|
ENST00000684953.1:n.2558G>T
|
|
|
ENST00000685090.1:n.1637G>T
|
|
|
ENST00000685232.1:n.1294G>T
|
|
|
ENST00000688574.1:n.1294G>T
|
|
|
ENST00000691124.1:n.2668G>T
|
|
|
ENST00000342988.8:c.1186G>T
MANE Select
|
ENSP00000341551.3:p.Asp396Tyr
|
|
ENST00000342988.7:c.1186G>T
|
ENSP00000341551.3:p.Asp396Tyr
|
|
ENST00000398417.6:c.1186G>T
|
ENSP00000381452.1:p.Asp396Tyr
|
|
ENST00000588745.5:c.898G>T
|
ENSP00000464901.1:p.Asp300Tyr
|
|
ENST00000590499.1:n.244G>T
|
|
|
ENST00000591126.5:n.3187G>T
|
|
|
ENST00000592186.5:c.955+7149G>T
|
ENSP00000468611.1:n.955+7149G>T
|
|
ENST00000611848.1:c.386G>T
|
|
|
NM_005359.5:c.1186G>T , LRG_318t1:c.1186G>T
|
NP_005350.1:p.Asp396Tyr
|
|
NM_005359.6:c.1186G>T
MANE Select
|
NP_005350.1:p.Asp396Tyr
|
|