ENST00000673913.2:c.*276G>T
|
ENSP00000501161.2:n.*276G>T
|
|
ENST00000710286.1:c.2293G>T
|
ENSP00000518176.1:p.Gly765Trp
|
|
ENST00000673903.1:c.1561G>T
|
ENSP00000501257.1:p.Gly521Trp
|
|
ENST00000673913.1:c.786G>T
|
ENSP00000501161.1:n.786G>T
|
|
ENST00000302118.5:c.1936G>T
MANE Select
|
ENSP00000303208.5:p.Gly646Trp
|
|
ENST00000490692.1:n.2482G>T
|
|
|
NM_174936.3:c.1936G>T , LRG_275t1:c.1936G>T
|
NP_777596.2:p.Gly646Trp
|
|
NR_110451.1:n.1543G>T
|
|
|
XM_011541193.1:c.1057G>T
|
XP_011539495.1:p.Gly353Trp
|
|
NM_174936.4:c.1936G>T
MANE Select
|
NP_777596.2:p.Gly646Trp
|
|
NR_110451.2:n.1543G>T
|
|
|