ENST00000673913.2:c.1626T>A
|
ENSP00000501161.2:p.Ala542=
|
|
ENST00000710286.1:c.1983T>A
|
ENSP00000518176.1:p.Ala661=
|
|
ENST00000673903.1:c.1251T>A
|
ENSP00000501257.1:p.Ala417=
|
|
ENST00000673913.1:c.366T>A
|
ENSP00000501161.1:p.Ala122=
|
|
ENST00000302118.5:c.1626T>A
MANE Select
|
ENSP00000303208.5:p.Ala542=
|
|
ENST00000490692.1:n.2227+961T>A
|
|
|
NM_174936.3:c.1626T>A , LRG_275t1:c.1626T>A
|
NP_777596.2:p.Ala542=
|
|
NR_110451.1:n.1233T>A
|
|
|
XM_011541193.1:c.747T>A
|
XP_011539495.1:p.Ala249=
|
|
NM_174936.4:c.1626T>A
MANE Select
|
NP_777596.2:p.Ala542=
|
|
NR_110451.2:n.1233T>A
|
|
|