ENST00000673913.2:c.*159G>C
|
ENSP00000501161.2:n.*159G>C
|
|
ENST00000710286.1:c.2176G>C
|
ENSP00000518176.1:p.Glu726Gln
|
|
ENST00000673903.1:c.1444G>C
|
ENSP00000501257.1:p.Glu482Gln
|
|
ENST00000673913.1:c.669G>C
|
ENSP00000501161.1:n.669G>C
|
|
ENST00000302118.5:c.1819G>C
MANE Select
|
ENSP00000303208.5:p.Glu607Gln
|
|
ENST00000490692.1:n.2365G>C
|
|
|
NM_174936.3:c.1819G>C , LRG_275t1:c.1819G>C
|
NP_777596.2:p.Glu607Gln
|
|
NR_110451.1:n.1426G>C
|
|
|
XM_011541193.1:c.940G>C
|
XP_011539495.1:p.Glu314Gln
|
|
NM_174936.4:c.1819G>C
MANE Select
|
NP_777596.2:p.Glu607Gln
|
|
NR_110451.2:n.1426G>C
|
|
|