ENST00000588860.6:c.*212G>T
|
ENSP00000465878.2:n.*212G>T
|
|
ENST00000589076.6:c.*212G>T
|
ENSP00000466934.2:n.*212G>T
|
|
ENST00000589941.2:c.*212G>T
|
ENSP00000465874.2:n.*212G>T
|
|
ENST00000590061.2:c.*212G>T
|
ENSP00000464772.2:n.*212G>T
|
|
ENST00000593223.2:c.*1868G>T
|
ENSP00000466118.2:n.*1868G>T
|
|
ENST00000611848.2:c.*523G>T
|
ENSP00000478613.2:n.*523G>T
|
|
ENST00000684953.1:n.3886G>T
|
|
|
ENST00000685090.1:n.3801G>T
|
|
|
ENST00000685232.1:n.2092G>T
|
|
|
ENST00000688574.1:n.1979G>T
|
|
|
ENST00000691124.1:n.4832G>T
|
|
|
ENST00000342988.8:c.*212G>T
MANE Select
|
ENSP00000341551.3:n.*212G>T
|
|
ENST00000342988.7:c.*212G>T
|
ENSP00000341551.3:n.*212G>T
|
|
ENST00000398417.6:c.*212G>T
|
ENSP00000381452.1:n.*212G>T
|
|
ENST00000586253.1:n.593G>T
|
|
|
ENST00000591126.5:n.3872G>T
|
|
|
ENST00000611848.1:c.1184G>T
|
|
|
NM_005359.5:c.*212G>T , LRG_318t1:c.*212G>T
|
NP_005350.1:n.*212G>T
|
|
NM_005359.6:c.*212G>T
MANE Select
|
NP_005350.1:n.*212G>T
|
|