|
ENST00000494804.2:n.3025G>T
|
|
|
|
ENST00000517337.2:c.1477G>T
|
ENSP00000429971.2:p.Glu493Ter
|
|
|
ENST00000523444.2:c.1477G>T
|
ENSP00000428252.2:p.Glu493Ter
|
|
|
ENST00000697292.1:c.1723G>T
|
ENSP00000513229.1:p.Glu575Ter
|
|
|
ENST00000697293.1:c.1723G>T
|
ENSP00000513230.1:p.Glu575Ter
|
|
|
ENST00000697294.1:c.*1334G>T
|
ENSP00000513231.1:n.*1334G>T
|
|
|
ENST00000697295.1:c.*1032G>T
|
ENSP00000513232.1:n.*1032G>T
|
|
|
ENST00000697296.1:c.*1391G>T
|
ENSP00000513233.1:n.*1391G>T
|
|
|
ENST00000697297.1:n.3508G>T
|
|
|
|
ENST00000697298.1:c.1477G>T
|
ENSP00000513234.1:p.Glu493Ter
|
|
|
ENST00000697299.1:c.1477G>T
|
ENSP00000513235.1:p.Glu493Ter
|
|
|
ENST00000697300.1:c.*1327G>T
|
ENSP00000513236.1:n.*1327G>T
|
|
|
ENST00000697301.1:c.*1244G>T
|
ENSP00000513237.1:n.*1244G>T
|
|
|
ENST00000697302.1:c.*1244G>T
|
ENSP00000513238.1:n.*1244G>T
|
|
|
ENST00000697303.1:c.*1327G>T
|
ENSP00000513239.1:n.*1327G>T
|
|
|
ENST00000697304.1:c.1411G>T
|
ENSP00000513240.1:p.Glu471Ter
|
|
|
ENST00000697306.1:c.*723G>T
|
ENSP00000513241.1:n.*723G>T
|
|
|
ENST00000697307.1:c.1723G>T
|
ENSP00000513242.1:p.Glu575Ter
|
|
|
ENST00000697308.1:c.1723G>T
|
ENSP00000513243.1:p.Glu575Ter
|
|
|
ENST00000697309.1:c.1723G>T
|
ENSP00000513244.1:p.Glu575Ter
|
|
|
ENST00000697310.1:c.1723G>T
|
ENSP00000513245.1:p.Glu575Ter
|
|
|
ENST00000697311.1:c.1723G>T
|
ENSP00000513246.1:p.Glu575Ter
|
|
|
ENST00000697312.1:c.*1121G>T
|
ENSP00000513247.1:n.*1121G>T
|
|
|
ENST00000697313.1:n.2687+16998G>T
|
|
|
|
ENST00000697314.1:n.3514G>T
|
|
|
|
ENST00000697315.1:c.1723G>T
|
ENSP00000513248.1:p.Glu575Ter
|
|
|
ENST00000697316.1:n.1844G>T
|
|
|
|
ENST00000697317.1:n.1833G>T
|
|
|
|
ENST00000697318.1:n.1835G>T
|
|
|
|
ENST00000265433.8:c.1723G>T
MANE Select
|
ENSP00000265433.4:p.Glu575Ter
|
|
|
ENST00000265433.7:c.1723G>T
|
ENSP00000265433.3:p.Glu575Ter
|
|
|
ENST00000396252.6:c.*1596G>T
|
ENSP00000379551.2:n.*1596G>T
|
|
|
ENST00000409330.5:c.1477G>T
|
ENSP00000386924.1:p.Glu493Ter
|
|
|
NM_001024688.2:c.1477G>T
|
NP_001019859.1:p.Glu493Ter
|
|
|
NM_002485.4:c.1723G>T , LRG_158t1:c.1723G>T
|
NP_002476.2:p.Glu575Ter
|
|
|
XM_011517044.1:c.1699G>T
|
XP_011515346.1:p.Glu567Ter
|
|
|
XM_011517045.1:c.1477G>T
|
XP_011515347.1:p.Glu493Ter
|
|
|
XR_928335.1:n.1862G>T
|
|
|
|
XM_017013460.1:c.844G>T
|
XP_016868949.1:p.Glu282Ter
|
|
|
XM_017013462.2:c.844G>T
|
XP_016868951.1:p.Glu282Ter
|
|
|
XM_024447163.1:c.1477G>T
|
XP_024302931.1:p.Glu493Ter
|
|
|
XM_024447164.1:c.1477G>T
|
XP_024302932.1:p.Glu493Ter
|
|
|
XM_024447165.1:c.844G>T
|
XP_024302933.1:p.Glu282Ter
|
|
|
NM_002485.5:c.1723G>T
MANE Select
|
NP_002476.2:p.Glu575Ter
|
|
|
NM_001024688.3:c.1477G>T
|
NP_001019859.1:p.Glu493Ter
|
|
