ENST00000673913.2:c.*361C>A
|
ENSP00000501161.2:n.*361C>A
|
|
ENST00000710286.1:c.2378C>A
|
ENSP00000518176.1:p.Ala793Asp
|
|
ENST00000673903.1:c.1646C>A
|
ENSP00000501257.1:p.Ala549Asp
|
|
ENST00000673913.1:c.871C>A
|
ENSP00000501161.1:n.871C>A
|
|
ENST00000302118.5:c.2021C>A
MANE Select
|
ENSP00000303208.5:p.Ala674Asp
|
|
ENST00000490692.1:n.2567C>A
|
|
|
NM_174936.3:c.2021C>A , LRG_275t1:c.2021C>A
|
NP_777596.2:p.Ala674Asp
|
|
NR_110451.1:n.1628C>A
|
|
|
XM_011541193.1:c.1142C>A
|
XP_011539495.1:p.Ala381Asp
|
|
NM_174936.4:c.2021C>A
MANE Select
|
NP_777596.2:p.Ala674Asp
|
|
NR_110451.2:n.1628C>A
|
|
|