ENST00000673913.2:c.*216T>G
|
ENSP00000501161.2:n.*216T>G
|
|
ENST00000710286.1:c.2233T>G
|
ENSP00000518176.1:p.Cys745Gly
|
|
ENST00000673903.1:c.1501T>G
|
ENSP00000501257.1:p.Cys501Gly
|
|
ENST00000673913.1:c.726T>G
|
ENSP00000501161.1:n.726T>G
|
|
ENST00000302118.5:c.1876T>G
MANE Select
|
ENSP00000303208.5:p.Cys626Gly
|
|
ENST00000490692.1:n.2422T>G
|
|
|
NM_174936.3:c.1876T>G , LRG_275t1:c.1876T>G
|
NP_777596.2:p.Cys626Gly
|
|
NR_110451.1:n.1483T>G
|
|
|
XM_011541193.1:c.997T>G
|
XP_011539495.1:p.Cys333Gly
|
|
NM_174936.4:c.1876T>G
MANE Select
|
NP_777596.2:p.Cys626Gly
|
|
NR_110451.2:n.1483T>G
|
|
|