ENST00000588860.6:c.1505G>C
|
ENSP00000465878.2:p.Arg502Thr
|
|
ENST00000589076.6:c.1505G>C
|
ENSP00000466934.2:p.Arg502Thr
|
|
ENST00000589941.2:c.1505G>C
|
ENSP00000465874.2:p.Arg502Thr
|
|
ENST00000590061.2:c.1505G>C
|
ENSP00000464772.2:p.Arg502Thr
|
|
ENST00000593223.2:c.*1502G>C
|
ENSP00000466118.2:n.*1502G>C
|
|
ENST00000611848.2:c.*157G>C
|
ENSP00000478613.2:n.*157G>C
|
|
ENST00000684953.1:n.3520G>C
|
|
|
ENST00000685090.1:n.3435G>C
|
|
|
ENST00000685232.1:n.1726G>C
|
|
|
ENST00000688574.1:n.1613G>C
|
|
|
ENST00000691124.1:n.4466G>C
|
|
|
ENST00000342988.8:c.1505G>C
MANE Select
|
ENSP00000341551.3:p.Arg502Thr
|
|
ENST00000342988.7:c.1505G>C
|
ENSP00000341551.3:p.Arg502Thr
|
|
ENST00000398417.6:c.1505G>C
|
ENSP00000381452.1:p.Arg502Thr
|
|
ENST00000586253.1:n.227G>C
|
|
|
ENST00000588745.5:c.1217G>C
|
ENSP00000464901.1:p.Arg406Thr
|
|
ENST00000591126.5:n.3506G>C
|
|
|
ENST00000592186.5:c.1152G>C
|
ENSP00000468611.1:n.1152G>C
|
|
ENST00000611848.1:c.818G>C
|
|
|
NM_005359.5:c.1505G>C , LRG_318t1:c.1505G>C
|
NP_005350.1:p.Arg502Thr
|
|
NM_005359.6:c.1505G>C
MANE Select
|
NP_005350.1:p.Arg502Thr
|
|