ENST00000470094.2:c.*563T>G
|
ENSP00000434898.2:n.*563T>G
|
|
ENST00000528762.2:c.*1407T>G
|
ENSP00000433168.2:n.*1407T>G
|
|
ENST00000530893.7:c.9671T>G
|
ENSP00000499438.2:p.Ile3224Arg
|
|
ENST00000665585.2:c.*1602T>G
|
ENSP00000499570.2:n.*1602T>G
|
|
ENST00000700202.2:c.9989T>G
|
ENSP00000514856.2:p.Ile3330Arg
|
|
ENST00000700202.1:c.2456T>G
|
ENSP00000514856.1:p.Ile819Arg
|
|
ENST00000700203.1:n.2167T>G
|
|
|
ENST00000380152.8:c.10040T>G
MANE Select
|
ENSP00000369497.3:p.Ile3347Arg
|
|
ENST00000544455.6:c.10040T>G
|
ENSP00000439902.1:p.Ile3347Arg
|
|
ENST00000614259.2:c.10048T>G
|
ENSP00000506251.1:n.10048T>G
|
|
ENST00000680887.1:c.10040T>G
|
ENSP00000505508.1:p.Ile3347Arg
|
|
ENST00000380152.7:c.10040T>G
|
ENSP00000369497.3:p.Ile3347Arg
|
|
ENST00000544455.5:c.10040T>G
|
ENSP00000439902.1:p.Ile3347Arg
|
|
NM_000059.3:c.10040T>G , LRG_293t1:c.10040T>G
|
NP_000050.2:p.Ile3347Arg
|
|
XM_011535203.1:c.10040T>G
|
XP_011533505.1:p.Ile3347Arg
|
|
XM_011535204.1:c.9944T>G
|
XP_011533506.1:p.Ile3315Arg
|
|
NM_000059.4:c.10040T>G
MANE Select
|
NP_000050.3:p.Ile3347Arg
|
|