ENST00000673913.2:c.*336A>T
|
ENSP00000501161.2:n.*336A>T
|
|
ENST00000710286.1:c.2353A>T
|
ENSP00000518176.1:p.Ser785Cys
|
|
ENST00000673903.1:c.1621A>T
|
ENSP00000501257.1:p.Ser541Cys
|
|
ENST00000673913.1:c.846A>T
|
ENSP00000501161.1:n.846A>T
|
|
ENST00000302118.5:c.1996A>T
MANE Select
|
ENSP00000303208.5:p.Ser666Cys
|
|
ENST00000490692.1:n.2542A>T
|
|
|
NM_174936.3:c.1996A>T , LRG_275t1:c.1996A>T
|
NP_777596.2:p.Ser666Cys
|
|
NR_110451.1:n.1603A>T
|
|
|
XM_011541193.1:c.1117A>T
|
XP_011539495.1:p.Ser373Cys
|
|
NM_174936.4:c.1996A>T
MANE Select
|
NP_777596.2:p.Ser666Cys
|
|
NR_110451.2:n.1603A>T
|
|
|