ENST00000673913.2:c.*162T>A
|
ENSP00000501161.2:n.*162T>A
|
|
ENST00000710286.1:c.2179T>A
|
ENSP00000518176.1:p.Cys727Ser
|
|
ENST00000673903.1:c.1447T>A
|
ENSP00000501257.1:p.Cys483Ser
|
|
ENST00000673913.1:c.672T>A
|
ENSP00000501161.1:n.672T>A
|
|
ENST00000302118.5:c.1822T>A
MANE Select
|
ENSP00000303208.5:p.Cys608Ser
|
|
ENST00000490692.1:n.2368T>A
|
|
|
NM_174936.3:c.1822T>A , LRG_275t1:c.1822T>A
|
NP_777596.2:p.Cys608Ser
|
|
NR_110451.1:n.1429T>A
|
|
|
XM_011541193.1:c.943T>A
|
XP_011539495.1:p.Cys315Ser
|
|
NM_174936.4:c.1822T>A
MANE Select
|
NP_777596.2:p.Cys608Ser
|
|
NR_110451.2:n.1429T>A
|
|
|