ENST00000673913.2:c.*206G>C
|
ENSP00000501161.2:n.*206G>C
|
|
ENST00000710286.1:c.2223G>C
|
ENSP00000518176.1:p.Val741=
|
|
ENST00000673903.1:c.1491G>C
|
ENSP00000501257.1:p.Val497=
|
|
ENST00000673913.1:c.716G>C
|
ENSP00000501161.1:n.716G>C
|
|
ENST00000302118.5:c.1866G>C
MANE Select
|
ENSP00000303208.5:p.Val622=
|
|
ENST00000490692.1:n.2412G>C
|
|
|
NM_174936.3:c.1866G>C , LRG_275t1:c.1866G>C
|
NP_777596.2:p.Val622=
|
|
NR_110451.1:n.1473G>C
|
|
|
XM_011541193.1:c.987G>C
|
XP_011539495.1:p.Val329=
|
|
NM_174936.4:c.1866G>C
MANE Select
|
NP_777596.2:p.Val622=
|
|
NR_110451.2:n.1473G>C
|
|
|