ENST00000684910.1:c.*100T>C
|
ENSP00000509844.1:n.*100T>C
|
|
ENST00000685439.1:c.222T>C
|
ENSP00000508454.1:p.Asn74=
|
|
ENST00000685944.1:c.567T>C
|
ENSP00000509266.1:p.Asn189=
|
|
ENST00000686212.1:n.169T>C
|
|
|
ENST00000687215.1:c.*322T>C
|
ENSP00000509706.1:n.*322T>C
|
|
ENST00000688152.1:c.*11T>C
|
ENSP00000509360.1:n.*11T>C
|
|
ENST00000688403.1:c.-178T>C
|
ENSP00000508944.1:n.-178T>C
|
|
ENST00000689314.1:c.612T>C
|
ENSP00000510607.1:p.Asn204=
|
|
ENST00000689694.1:c.567T>C
|
ENSP00000508718.1:p.Asn189=
|
|
ENST00000689810.1:c.*216T>C
|
ENSP00000510635.1:n.*216T>C
|
|
ENST00000690282.1:c.-178T>C
|
ENSP00000509809.1:n.-178T>C
|
|
ENST00000690351.1:c.*219T>C
|
ENSP00000509728.1:n.*219T>C
|
|
ENST00000691232.1:c.222T>C
|
ENSP00000509675.1:p.Asn74=
|
|
ENST00000691482.1:n.1582T>C
|
|
|
ENST00000691686.1:c.567T>C
|
ENSP00000509784.1:p.Asn189=
|
|
ENST00000691851.1:c.567T>C
|
ENSP00000510106.1:p.Asn189=
|
|
ENST00000692015.1:c.354T>C
|
ENSP00000510634.1:p.Asn118=
|
|
ENST00000692638.1:c.*372T>C
|
ENSP00000509412.1:n.*372T>C
|
|
ENST00000692852.1:c.567T>C
|
ENSP00000510337.1:p.Asn189=
|
|
ENST00000692915.1:c.*774T>C
|
ENSP00000508547.1:n.*774T>C
|
|
ENST00000370396.7:c.567T>C
MANE Select
|
ENSP00000359423.3:p.Asn189=
|
|
ENST00000306167.11:n.434T>C
|
|
|
ENST00000370396.6:c.567T>C
|
ENSP00000359423.2:p.Asn189=
|
|
ENST00000490530.1:n.506T>C
|
|
|
NM_000252.2:c.567T>C , LRG_839t1:c.567T>C
|
NP_000243.1:p.Asn189=
|
|
XM_005274687.2:c.567T>C
|
XP_005274744.1:p.Asn189=
|
|
XM_011531170.1:c.633T>C
|
XP_011529472.1:p.Asn211=
|
|
XM_011531171.1:c.612T>C
|
XP_011529473.1:p.Asn204=
|
|
XM_011531172.1:c.612T>C
|
XP_011529474.1:p.Asn204=
|
|
XM_011531173.1:c.567T>C
|
XP_011529475.1:p.Asn189=
|
|
XM_011531173.2:c.567T>C
|
XP_011529475.1:p.Asn189=
|
|
XM_017029547.1:c.612T>C
|
XP_016885036.1:p.Asn204=
|
|
XM_017029548.1:c.612T>C
|
XP_016885037.1:p.Asn204=
|
|
XM_017029549.1:c.567T>C
|
XP_016885038.1:p.Asn189=
|
|
XM_017029550.1:c.456T>C
|
XP_016885039.1:p.Asn152=
|
|
XM_017029551.2:c.-178T>C
|
XP_016885040.1:n.-178T>C
|
|
NM_000252.3:c.567T>C
MANE Select
|
NP_000243.1:p.Asn189=
|
|
NM_001376906.1:c.567T>C
|
NP_001363835.1:p.Asn189=
|
|
NM_001376907.1:c.456T>C
|
NP_001363836.1:p.Asn152=
|
|
NM_001376908.1:c.567T>C
|
NP_001363837.1:p.Asn189=
|
|