ENST00000673913.2:c.*107G>A
|
ENSP00000501161.2:n.*107G>A
|
|
ENST00000710286.1:c.2124G>A
|
ENSP00000518176.1:p.Val708=
|
|
ENST00000673903.1:c.1392G>A
|
ENSP00000501257.1:p.Val464=
|
|
ENST00000673913.1:c.617G>A
|
ENSP00000501161.1:n.617G>A
|
|
ENST00000302118.5:c.1767G>A
MANE Select
|
ENSP00000303208.5:p.Val589=
|
|
ENST00000490692.1:n.2313G>A
|
|
|
NM_174936.3:c.1767G>A , LRG_275t1:c.1767G>A
|
NP_777596.2:p.Val589=
|
|
NR_110451.1:n.1374G>A
|
|
|
XM_011541193.1:c.888G>A
|
XP_011539495.1:p.Val296=
|
|
NM_174936.4:c.1767G>A
MANE Select
|
NP_777596.2:p.Val589=
|
|
NR_110451.2:n.1374G>A
|
|
|