ENST00000588860.6:c.*116G>C
|
ENSP00000465878.2:n.*116G>C
|
|
ENST00000589076.6:c.*116G>C
|
ENSP00000466934.2:n.*116G>C
|
|
ENST00000589941.2:c.*116G>C
|
ENSP00000465874.2:n.*116G>C
|
|
ENST00000590061.2:c.*116G>C
|
ENSP00000464772.2:n.*116G>C
|
|
ENST00000593223.2:c.*1772G>C
|
ENSP00000466118.2:n.*1772G>C
|
|
ENST00000611848.2:c.*427G>C
|
ENSP00000478613.2:n.*427G>C
|
|
ENST00000684953.1:n.3790G>C
|
|
|
ENST00000685090.1:n.3705G>C
|
|
|
ENST00000685232.1:n.1996G>C
|
|
|
ENST00000688574.1:n.1883G>C
|
|
|
ENST00000691124.1:n.4736G>C
|
|
|
ENST00000342988.8:c.*116G>C
MANE Select
|
ENSP00000341551.3:n.*116G>C
|
|
ENST00000342988.7:c.*116G>C
|
ENSP00000341551.3:n.*116G>C
|
|
ENST00000398417.6:c.*116G>C
|
ENSP00000381452.1:n.*116G>C
|
|
ENST00000586253.1:n.497G>C
|
|
|
ENST00000591126.5:n.3776G>C
|
|
|
ENST00000611848.1:c.1088G>C
|
|
|
NM_005359.5:c.*116G>C , LRG_318t1:c.*116G>C
|
NP_005350.1:n.*116G>C
|
|
NM_005359.6:c.*116G>C
MANE Select
|
NP_005350.1:n.*116G>C
|
|