ENST00000673913.2:c.*143C>G
|
ENSP00000501161.2:n.*143C>G
|
|
ENST00000710286.1:c.2160C>G
|
ENSP00000518176.1:p.Cys720Trp
|
|
ENST00000673903.1:c.1428C>G
|
ENSP00000501257.1:p.Cys476Trp
|
|
ENST00000673913.1:c.653C>G
|
ENSP00000501161.1:n.653C>G
|
|
ENST00000302118.5:c.1803C>G
MANE Select
|
ENSP00000303208.5:p.Cys601Trp
|
|
ENST00000490692.1:n.2349C>G
|
|
|
NM_174936.3:c.1803C>G , LRG_275t1:c.1803C>G
|
NP_777596.2:p.Cys601Trp
|
|
NR_110451.1:n.1410C>G
|
|
|
XM_011541193.1:c.924C>G
|
XP_011539495.1:p.Cys308Trp
|
|
NM_174936.4:c.1803C>G
MANE Select
|
NP_777596.2:p.Cys601Trp
|
|
NR_110451.2:n.1410C>G
|
|
|