ENST00000470094.2:c.*189T>A
|
ENSP00000434898.2:n.*189T>A
|
|
ENST00000528762.2:c.*1033T>A
|
ENSP00000433168.2:n.*1033T>A
|
|
ENST00000530893.7:c.9297T>A
|
ENSP00000499438.2:p.Cys3099Ter
|
|
ENST00000665585.2:c.*1228T>A
|
ENSP00000499570.2:n.*1228T>A
|
|
ENST00000700202.2:c.9615T>A
|
ENSP00000514856.2:p.Cys3205Ter
|
|
ENST00000700202.1:c.2082T>A
|
ENSP00000514856.1:p.Cys694Ter
|
|
ENST00000700203.1:n.1793T>A
|
|
|
ENST00000380152.8:c.9666T>A
MANE Select
|
ENSP00000369497.3:p.Cys3222Ter
|
|
ENST00000544455.6:c.9666T>A
|
ENSP00000439902.1:p.Cys3222Ter
|
|
ENST00000614259.2:c.9674T>A
|
ENSP00000506251.1:n.9674T>A
|
|
ENST00000665585.1:c.2544T>A
|
|
|
ENST00000680887.1:c.9666T>A
|
ENSP00000505508.1:p.Cys3222Ter
|
|
ENST00000380152.7:c.9666T>A
|
ENSP00000369497.3:p.Cys3222Ter
|
|
ENST00000470094.1:c.749T>A
|
|
|
ENST00000533776.1:n.254T>A
|
|
|
ENST00000544455.5:c.9666T>A
|
ENSP00000439902.1:p.Cys3222Ter
|
|
NM_000059.3:c.9666T>A , LRG_293t1:c.9666T>A
|
NP_000050.2:p.Cys3222Ter
|
|
XM_011535203.1:c.9666T>A
|
XP_011533505.1:p.Cys3222Ter
|
|
XM_011535204.1:c.9570T>A
|
XP_011533506.1:p.Cys3190Ter
|
|
NM_000059.4:c.9666T>A
MANE Select
|
NP_000050.3:p.Cys3222Ter
|
|