ENST00000673913.2:c.1582C>G
|
ENSP00000501161.2:p.Leu528Val
|
|
ENST00000710286.1:c.1939C>G
|
ENSP00000518176.1:p.Leu647Val
|
|
ENST00000673903.1:c.1207C>G
|
ENSP00000501257.1:p.Leu403Val
|
|
ENST00000673913.1:c.322C>G
|
ENSP00000501161.1:p.Leu108Val
|
|
ENST00000302118.5:c.1582C>G
MANE Select
|
ENSP00000303208.5:p.Leu528Val
|
|
ENST00000490692.1:n.2227+917C>G
|
|
|
NM_174936.3:c.1582C>G , LRG_275t1:c.1582C>G
|
NP_777596.2:p.Leu528Val
|
|
NR_110451.1:n.1189C>G
|
|
|
XM_011541193.1:c.703C>G
|
XP_011539495.1:p.Leu235Val
|
|
NM_174936.4:c.1582C>G
MANE Select
|
NP_777596.2:p.Leu528Val
|
|
NR_110451.2:n.1189C>G
|
|
|