ENST00000588860.6:c.1487G>T
|
ENSP00000465878.2:p.Arg496Leu
|
|
ENST00000589076.6:c.1487G>T
|
ENSP00000466934.2:p.Arg496Leu
|
|
ENST00000589941.2:c.1487G>T
|
ENSP00000465874.2:p.Arg496Leu
|
|
ENST00000590061.2:c.1487G>T
|
ENSP00000464772.2:p.Arg496Leu
|
|
ENST00000593223.2:c.*1484G>T
|
ENSP00000466118.2:n.*1484G>T
|
|
ENST00000611848.2:c.*139G>T
|
ENSP00000478613.2:n.*139G>T
|
|
ENST00000684953.1:n.3502G>T
|
|
|
ENST00000685090.1:n.3417G>T
|
|
|
ENST00000685232.1:n.1708G>T
|
|
|
ENST00000688574.1:n.1595G>T
|
|
|
ENST00000691124.1:n.4448G>T
|
|
|
ENST00000342988.8:c.1487G>T
MANE Select
|
ENSP00000341551.3:p.Arg496Leu
|
|
ENST00000342988.7:c.1487G>T
|
ENSP00000341551.3:p.Arg496Leu
|
|
ENST00000398417.6:c.1487G>T
|
ENSP00000381452.1:p.Arg496Leu
|
|
ENST00000586253.1:n.209G>T
|
|
|
ENST00000588745.5:c.1199G>T
|
ENSP00000464901.1:p.Arg400Leu
|
|
ENST00000591126.5:n.3488G>T
|
|
|
ENST00000592186.5:c.1134G>T
|
ENSP00000468611.1:n.1134G>T
|
|
ENST00000611848.1:c.800G>T
|
|
|
NM_005359.5:c.1487G>T , LRG_318t1:c.1487G>T
|
NP_005350.1:p.Arg496Leu
|
|
NM_005359.6:c.1487G>T
MANE Select
|
NP_005350.1:p.Arg496Leu
|
|