ENST00000470094.2:c.*545A>T
|
ENSP00000434898.2:n.*545A>T
|
|
ENST00000528762.2:c.*1389A>T
|
ENSP00000433168.2:n.*1389A>T
|
|
ENST00000530893.7:c.9653A>T
|
ENSP00000499438.2:p.Asp3218Val
|
|
ENST00000665585.2:c.*1584A>T
|
ENSP00000499570.2:n.*1584A>T
|
|
ENST00000700202.2:c.9971A>T
|
ENSP00000514856.2:p.Asp3324Val
|
|
ENST00000700202.1:c.2438A>T
|
ENSP00000514856.1:p.Asp813Val
|
|
ENST00000700203.1:n.2149A>T
|
|
|
ENST00000380152.8:c.10022A>T
MANE Select
|
ENSP00000369497.3:p.Asp3341Val
|
|
ENST00000544455.6:c.10022A>T
|
ENSP00000439902.1:p.Asp3341Val
|
|
ENST00000614259.2:c.10030A>T
|
ENSP00000506251.1:n.10030A>T
|
|
ENST00000680887.1:c.10022A>T
|
ENSP00000505508.1:p.Asp3341Val
|
|
ENST00000380152.7:c.10022A>T
|
ENSP00000369497.3:p.Asp3341Val
|
|
ENST00000544455.5:c.10022A>T
|
ENSP00000439902.1:p.Asp3341Val
|
|
NM_000059.3:c.10022A>T , LRG_293t1:c.10022A>T
|
NP_000050.2:p.Asp3341Val
|
|
XM_011535203.1:c.10022A>T
|
XP_011533505.1:p.Asp3341Val
|
|
XM_011535204.1:c.9926A>T
|
XP_011533506.1:p.Asp3309Val
|
|
NM_000059.4:c.10022A>T
MANE Select
|
NP_000050.3:p.Asp3341Val
|
|