ENST00000673913.2:c.*169T>G
|
ENSP00000501161.2:n.*169T>G
|
|
ENST00000710286.1:c.2186T>G
|
ENSP00000518176.1:p.Val729Gly
|
|
ENST00000673903.1:c.1454T>G
|
ENSP00000501257.1:p.Val485Gly
|
|
ENST00000673913.1:c.679T>G
|
ENSP00000501161.1:n.679T>G
|
|
ENST00000302118.5:c.1829T>G
MANE Select
|
ENSP00000303208.5:p.Val610Gly
|
|
ENST00000490692.1:n.2375T>G
|
|
|
NM_174936.3:c.1829T>G , LRG_275t1:c.1829T>G
|
NP_777596.2:p.Val610Gly
|
|
NR_110451.1:n.1436T>G
|
|
|
XM_011541193.1:c.950T>G
|
XP_011539495.1:p.Val317Gly
|
|
NM_174936.4:c.1829T>G
MANE Select
|
NP_777596.2:p.Val610Gly
|
|
NR_110451.2:n.1436T>G
|
|
|