ENST00000673913.2:c.*115G>T
|
ENSP00000501161.2:n.*115G>T
|
|
ENST00000710286.1:c.2132G>T
|
ENSP00000518176.1:p.Arg711Met
|
|
ENST00000673903.1:c.1400G>T
|
ENSP00000501257.1:p.Arg467Met
|
|
ENST00000673913.1:c.625G>T
|
ENSP00000501161.1:n.625G>T
|
|
ENST00000302118.5:c.1775G>T
MANE Select
|
ENSP00000303208.5:p.Arg592Met
|
|
ENST00000490692.1:n.2321G>T
|
|
|
NM_174936.3:c.1775G>T , LRG_275t1:c.1775G>T
|
NP_777596.2:p.Arg592Met
|
|
NR_110451.1:n.1382G>T
|
|
|
XM_011541193.1:c.896G>T
|
XP_011539495.1:p.Arg299Met
|
|
NM_174936.4:c.1775G>T
MANE Select
|
NP_777596.2:p.Arg592Met
|
|
NR_110451.2:n.1382G>T
|
|
|