ENST00000588860.6:c.1508T>C
|
ENSP00000465878.2:p.Met503Thr
|
|
ENST00000589076.6:c.1508T>C
|
ENSP00000466934.2:p.Met503Thr
|
|
ENST00000589941.2:c.1508T>C
|
ENSP00000465874.2:p.Met503Thr
|
|
ENST00000590061.2:c.1508T>C
|
ENSP00000464772.2:p.Met503Thr
|
|
ENST00000593223.2:c.*1505T>C
|
ENSP00000466118.2:n.*1505T>C
|
|
ENST00000611848.2:c.*160T>C
|
ENSP00000478613.2:n.*160T>C
|
|
ENST00000684953.1:n.3523T>C
|
|
|
ENST00000685090.1:n.3438T>C
|
|
|
ENST00000685232.1:n.1729T>C
|
|
|
ENST00000688574.1:n.1616T>C
|
|
|
ENST00000691124.1:n.4469T>C
|
|
|
ENST00000342988.8:c.1508T>C
MANE Select
|
ENSP00000341551.3:p.Met503Thr
|
|
ENST00000342988.7:c.1508T>C
|
ENSP00000341551.3:p.Met503Thr
|
|
ENST00000398417.6:c.1508T>C
|
ENSP00000381452.1:p.Met503Thr
|
|
ENST00000586253.1:n.230T>C
|
|
|
ENST00000588745.5:c.1220T>C
|
ENSP00000464901.1:p.Met407Thr
|
|
ENST00000591126.5:n.3509T>C
|
|
|
ENST00000592186.5:c.1155T>C
|
ENSP00000468611.1:n.1155T>C
|
|
ENST00000611848.1:c.821T>C
|
|
|
NM_005359.5:c.1508T>C , LRG_318t1:c.1508T>C
|
NP_005350.1:p.Met503Thr
|
|
NM_005359.6:c.1508T>C
MANE Select
|
NP_005350.1:p.Met503Thr
|
|