ENST00000673913.2:c.*215C>G
|
ENSP00000501161.2:n.*215C>G
|
|
ENST00000710286.1:c.2232C>G
|
ENSP00000518176.1:p.Ala744=
|
|
ENST00000673903.1:c.1500C>G
|
ENSP00000501257.1:p.Ala500=
|
|
ENST00000673913.1:c.725C>G
|
ENSP00000501161.1:n.725C>G
|
|
ENST00000302118.5:c.1875C>G
MANE Select
|
ENSP00000303208.5:p.Ala625=
|
|
ENST00000490692.1:n.2421C>G
|
|
|
NM_174936.3:c.1875C>G , LRG_275t1:c.1875C>G
|
NP_777596.2:p.Ala625=
|
|
NR_110451.1:n.1482C>G
|
|
|
XM_011541193.1:c.996C>G
|
XP_011539495.1:p.Ala332=
|
|
NM_174936.4:c.1875C>G
MANE Select
|
NP_777596.2:p.Ala625=
|
|
NR_110451.2:n.1482C>G
|
|
|