ENST00000684910.1:c.*646G>A
|
ENSP00000509844.1:n.*646G>A
|
|
ENST00000685439.1:c.768G>A
|
ENSP00000508454.1:p.Val256=
|
|
ENST00000685944.1:c.1113G>A
|
ENSP00000509266.1:p.Val371=
|
|
ENST00000686212.1:n.715G>A
|
|
|
ENST00000687215.1:c.*868G>A
|
ENSP00000509706.1:n.*868G>A
|
|
ENST00000688152.1:c.*557G>A
|
ENSP00000509360.1:n.*557G>A
|
|
ENST00000688403.1:c.369G>A
|
ENSP00000508944.1:p.Val123=
|
|
ENST00000689314.1:c.1158G>A
|
ENSP00000510607.1:p.Val386=
|
|
ENST00000689694.1:c.1113G>A
|
ENSP00000508718.1:p.Val371=
|
|
ENST00000689810.1:c.*762G>A
|
ENSP00000510635.1:n.*762G>A
|
|
ENST00000690282.1:c.369G>A
|
ENSP00000509809.1:p.Val123=
|
|
ENST00000690351.1:c.*765G>A
|
ENSP00000509728.1:n.*765G>A
|
|
ENST00000691232.1:c.768G>A
|
ENSP00000509675.1:p.Val256=
|
|
ENST00000691482.1:n.2128G>A
|
|
|
ENST00000691686.1:c.1113G>A
|
ENSP00000509784.1:p.Val371=
|
|
ENST00000691851.1:c.1053+7979G>A
|
ENSP00000510106.1:n.1053+7979G>A
|
|
ENST00000692015.1:c.900G>A
|
ENSP00000510634.1:p.Val300=
|
|
ENST00000692638.1:c.*918G>A
|
ENSP00000509412.1:n.*918G>A
|
|
ENST00000692852.1:c.924G>A
|
ENSP00000510337.1:p.Val308=
|
|
ENST00000692915.1:c.*1259G>A
|
ENSP00000508547.1:n.*1259G>A
|
|
ENST00000370396.7:c.1113G>A
MANE Select
|
ENSP00000359423.3:p.Val371=
|
|
ENST00000306167.11:n.980G>A
|
|
|
ENST00000370396.6:c.1113G>A
|
ENSP00000359423.2:p.Val371=
|
|
NM_000252.2:c.1113G>A , LRG_839t1:c.1113G>A
|
NP_000243.1:p.Val371=
|
|
XM_005274687.2:c.1113G>A
|
XP_005274744.1:p.Val371=
|
|
XM_011531170.1:c.1179G>A
|
XP_011529472.1:p.Val393=
|
|
XM_011531171.1:c.1158G>A
|
XP_011529473.1:p.Val386=
|
|
XM_011531172.1:c.1158G>A
|
XP_011529474.1:p.Val386=
|
|
XM_011531173.1:c.1113G>A
|
XP_011529475.1:p.Val371=
|
|
XM_011531173.2:c.1113G>A
|
XP_011529475.1:p.Val371=
|
|
XM_017029547.1:c.1158G>A
|
XP_016885036.1:p.Val386=
|
|
XM_017029548.1:c.1158G>A
|
XP_016885037.1:p.Val386=
|
|
XM_017029549.1:c.1113G>A
|
XP_016885038.1:p.Val371=
|
|
XM_017029550.1:c.1002G>A
|
XP_016885039.1:p.Val334=
|
|
XM_017029551.2:c.369G>A
|
XP_016885040.1:p.Val123=
|
|
NM_000252.3:c.1113G>A
MANE Select
|
NP_000243.1:p.Val371=
|
|
NM_001376906.1:c.1113G>A
|
NP_001363835.1:p.Val371=
|
|
NM_001376907.1:c.1002G>A
|
NP_001363836.1:p.Val334=
|
|
NM_001376908.1:c.1113G>A
|
NP_001363837.1:p.Val371=
|
|