ENST00000673913.2:c.*356G>T
|
ENSP00000501161.2:n.*356G>T
|
|
ENST00000710286.1:c.2373G>T
|
ENSP00000518176.1:p.Val791=
|
|
ENST00000673903.1:c.1641G>T
|
ENSP00000501257.1:p.Val547=
|
|
ENST00000673913.1:c.866G>T
|
ENSP00000501161.1:n.866G>T
|
|
ENST00000302118.5:c.2016G>T
MANE Select
|
ENSP00000303208.5:p.Val672=
|
|
ENST00000490692.1:n.2562G>T
|
|
|
NM_174936.3:c.2016G>T , LRG_275t1:c.2016G>T
|
NP_777596.2:p.Val672=
|
|
NR_110451.1:n.1623G>T
|
|
|
XM_011541193.1:c.1137G>T
|
XP_011539495.1:p.Val379=
|
|
NM_174936.4:c.2016G>T
MANE Select
|
NP_777596.2:p.Val672=
|
|
NR_110451.2:n.1623G>T
|
|
|