|
ENST00000494804.2:n.2701G>T
|
|
|
|
ENST00000517337.2:c.1153G>T
|
ENSP00000429971.2:p.Glu385Ter
|
|
|
ENST00000523444.2:c.1153G>T
|
ENSP00000428252.2:p.Glu385Ter
|
|
|
ENST00000697292.1:c.1399G>T
|
ENSP00000513229.1:p.Glu467Ter
|
|
|
ENST00000697293.1:c.1399G>T
|
ENSP00000513230.1:p.Glu467Ter
|
|
|
ENST00000697294.1:c.*1010G>T
|
ENSP00000513231.1:n.*1010G>T
|
|
|
ENST00000697295.1:c.*708G>T
|
ENSP00000513232.1:n.*708G>T
|
|
|
ENST00000697296.1:c.*1067G>T
|
ENSP00000513233.1:n.*1067G>T
|
|
|
ENST00000697297.1:n.3184G>T
|
|
|
|
ENST00000697298.1:c.1153G>T
|
ENSP00000513234.1:p.Glu385Ter
|
|
|
ENST00000697299.1:c.1153G>T
|
ENSP00000513235.1:p.Glu385Ter
|
|
|
ENST00000697300.1:c.*1003G>T
|
ENSP00000513236.1:n.*1003G>T
|
|
|
ENST00000697301.1:c.*920G>T
|
ENSP00000513237.1:n.*920G>T
|
|
|
ENST00000697302.1:c.*920G>T
|
ENSP00000513238.1:n.*920G>T
|
|
|
ENST00000697303.1:c.*1003G>T
|
ENSP00000513239.1:n.*1003G>T
|
|
|
ENST00000697304.1:c.1087G>T
|
ENSP00000513240.1:p.Glu363Ter
|
|
|
ENST00000697306.1:c.*399G>T
|
ENSP00000513241.1:n.*399G>T
|
|
|
ENST00000697307.1:c.1399G>T
|
ENSP00000513242.1:p.Glu467Ter
|
|
|
ENST00000697308.1:c.1399G>T
|
ENSP00000513243.1:p.Glu467Ter
|
|
|
ENST00000697309.1:c.1399G>T
|
ENSP00000513244.1:p.Glu467Ter
|
|
|
ENST00000697310.1:c.1399G>T
|
ENSP00000513245.1:p.Glu467Ter
|
|
|
ENST00000697311.1:c.1399G>T
|
ENSP00000513246.1:p.Glu467Ter
|
|
|
ENST00000697312.1:c.*797G>T
|
ENSP00000513247.1:n.*797G>T
|
|
|
ENST00000697313.1:n.2687+16674G>T
|
|
|
|
ENST00000697314.1:n.3190G>T
|
|
|
|
ENST00000697315.1:c.1399G>T
|
ENSP00000513248.1:p.Glu467Ter
|
|
|
ENST00000697316.1:n.1520G>T
|
|
|
|
ENST00000697317.1:n.1509G>T
|
|
|
|
ENST00000697318.1:n.1511G>T
|
|
|
|
ENST00000265433.8:c.1399G>T
MANE Select
|
ENSP00000265433.4:p.Glu467Ter
|
|
|
ENST00000265433.7:c.1399G>T
|
ENSP00000265433.3:p.Glu467Ter
|
|
|
ENST00000396252.6:c.*1272G>T
|
ENSP00000379551.2:n.*1272G>T
|
|
|
ENST00000409330.5:c.1153G>T
|
ENSP00000386924.1:p.Glu385Ter
|
|
|
NM_001024688.2:c.1153G>T
|
NP_001019859.1:p.Glu385Ter
|
|
|
NM_002485.4:c.1399G>T , LRG_158t1:c.1399G>T
|
NP_002476.2:p.Glu467Ter
|
|
|
XM_011517044.1:c.1375G>T
|
XP_011515346.1:p.Glu459Ter
|
|
|
XM_011517045.1:c.1153G>T
|
XP_011515347.1:p.Glu385Ter
|
|
|
XM_011517046.1:c.1400G>T
|
XP_011515348.1:p.Gly467Val
|
|
|
XR_928335.1:n.1538G>T
|
|
|
|
XM_017013460.1:c.520G>T
|
XP_016868949.1:p.Glu174Ter
|
|
|
XM_017013462.2:c.520G>T
|
XP_016868951.1:p.Glu174Ter
|
|
|
XM_024447163.1:c.1153G>T
|
XP_024302931.1:p.Glu385Ter
|
|
|
XM_024447164.1:c.1153G>T
|
XP_024302932.1:p.Glu385Ter
|
|
|
XM_024447165.1:c.520G>T
|
XP_024302933.1:p.Glu174Ter
|
|
|
NM_002485.5:c.1399G>T
MANE Select
|
NP_002476.2:p.Glu467Ter
|
|
|
NM_001024688.3:c.1153G>T
|
NP_001019859.1:p.Glu385Ter
|
|
