ENST00000673913.2:c.*127T>C
|
ENSP00000501161.2:n.*127T>C
|
|
ENST00000710286.1:c.2144T>C
|
ENSP00000518176.1:p.Ile715Thr
|
|
ENST00000673903.1:c.1412T>C
|
ENSP00000501257.1:p.Ile471Thr
|
|
ENST00000673913.1:c.637T>C
|
ENSP00000501161.1:n.637T>C
|
|
ENST00000302118.5:c.1787T>C
MANE Select
|
ENSP00000303208.5:p.Ile596Thr
|
|
ENST00000490692.1:n.2333T>C
|
|
|
NM_174936.3:c.1787T>C , LRG_275t1:c.1787T>C
|
NP_777596.2:p.Ile596Thr
|
|
NR_110451.1:n.1394T>C
|
|
|
XM_011541193.1:c.908T>C
|
XP_011539495.1:p.Ile303Thr
|
|
NM_174936.4:c.1787T>C
MANE Select
|
NP_777596.2:p.Ile596Thr
|
|
NR_110451.2:n.1394T>C
|
|
|