ENST00000568566.6:c.*3763A>T
|
ENSP00000455997.2:n.*3763A>T
|
|
ENST00000642206.2:c.5261A>T
|
ENSP00000495146.2:p.Glu1754Val
|
|
ENST00000642365.2:c.5411A>T
|
ENSP00000495459.2:p.Glu1804Val
|
|
ENST00000644417.2:c.*5927A>T
|
ENSP00000493912.2:n.*5927A>T
|
|
ENST00000646464.2:c.*8163A>T
|
ENSP00000496610.2:n.*8163A>T
|
|
ENST00000219476.9:c.5414A>T
MANE Select
|
ENSP00000219476.3:p.Glu1805Val
|
|
ENST00000350773.9:c.5345A>T
|
ENSP00000344383.4:p.Glu1782Val
|
|
ENST00000401874.7:c.5213A>T
|
ENSP00000384468.2:p.Glu1738Val
|
|
ENST00000568454.6:c.5246A>T
|
ENSP00000454487.1:p.Glu1749Val
|
|
ENST00000569110.2:c.1637A>T
|
|
|
ENST00000569930.2:n.3296A>T
|
|
|
ENST00000642365.1:c.4068A>T
|
|
|
ENST00000642561.1:c.5273A>T
|
ENSP00000495099.1:p.Glu1758Val
|
|
ENST00000642791.1:n.1011A>T
|
|
|
ENST00000642797.1:c.5216A>T
|
ENSP00000493846.1:p.Glu1739Val
|
|
ENST00000642936.1:c.5282A>T
|
ENSP00000494514.1:p.Glu1761Val
|
|
ENST00000643088.1:c.5207A>T
|
ENSP00000494747.1:p.Glu1736Val
|
|
ENST00000643426.1:n.3062A>T
|
|
|
ENST00000643946.1:c.5339A>T
|
ENSP00000495927.1:p.Glu1780Val
|
|
ENST00000644043.1:c.5285A>T
|
ENSP00000496262.1:p.Glu1762Val
|
|
ENST00000644329.1:c.5300A>T
|
ENSP00000496611.1:p.Glu1767Val
|
|
ENST00000644335.1:c.5210A>T
|
ENSP00000496317.1:p.Glu1737Val
|
|
ENST00000644399.1:c.5335A>T
|
|
|
ENST00000646388.1:c.5408A>T
|
ENSP00000495921.1:p.Glu1803Val
|
|
ENST00000646634.1:n.4229A>T
|
|
|
ENST00000646674.1:n.2666A>T
|
|
|
ENST00000647042.1:n.2637A>T
|
|
|
ENST00000647180.1:n.2527A>T
|
|
|
ENST00000219476.7:c.5414A>T
|
ENSP00000219476.3:p.Glu1805Val
|
|
ENST00000350773.8:c.5345A>T
|
ENSP00000344383.4:p.Glu1782Val
|
|
ENST00000382538.10:c.5069A>T
|
ENSP00000371978.6:p.Glu1690Val
|
|
ENST00000401874.6:c.5213A>T
|
ENSP00000384468.2:p.Glu1738Val
|
|
ENST00000439117.6:c.*4581A>T
|
ENSP00000406980.2:n.*4581A>T
|
|
ENST00000439673.6:c.5105A>T
|
ENSP00000399232.2:p.Glu1702Val
|
|
ENST00000497886.5:n.3137A>T
|
|
|
ENST00000568454.5:c.5246A>T
|
ENSP00000454487.1:p.Glu1749Val
|
|
ENST00000569110.1:c.1596A>T
|
|
|
ENST00000569930.1:n.2529A>T
|
|
|
NM_000548.3:c.5414A>T , LRG_487t1:c.5414A>T
|
NP_000539.2:p.Glu1805Val
|
|
NM_001077183.1:c.5213A>T
|
NP_001070651.1:p.Glu1738Val
|
|
NM_001114382.1:c.5345A>T
|
NP_001107854.1:p.Glu1782Val
|
|
XM_005255529.3:c.5285A>T
|
XP_005255586.2:p.Glu1762Val
|
|
XM_005255531.3:c.5216A>T
|
XP_005255588.2:p.Glu1739Val
|
|
XM_011522636.1:c.5468A>T
|
XP_011520938.1:p.Glu1823Val
|
|
XM_011522637.1:c.5465A>T
|
XP_011520939.1:p.Glu1822Val
|
|
XM_011522638.1:c.5357A>T
|
XP_011520940.1:p.Glu1786Val
|
|
XM_011522639.1:c.5339A>T
|
XP_011520941.1:p.Glu1780Val
|
|
XM_011522640.1:c.5336A>T
|
XP_011520942.1:p.Glu1779Val
|
|
XM_011522641.1:c.5105A>T
|
XP_011520943.1:p.Glu1702Val
|
|
NM_000548.4:c.5414A>T
|
NP_000539.2:p.Glu1805Val
|
|
NM_001077183.2:c.5213A>T
|
NP_001070651.1:p.Glu1738Val
|
|
NM_001114382.2:c.5345A>T
|
NP_001107854.1:p.Glu1782Val
|
|
NM_001318827.1:c.5105A>T
|
NP_001305756.1:p.Glu1702Val
|
|
NM_001318829.1:c.5069A>T
|
NP_001305758.1:p.Glu1690Val
|
|
NM_001318831.1:c.4682A>T
|
NP_001305760.1:p.Glu1561Val
|
|
NM_001318832.1:c.5246A>T
|
NP_001305761.1:p.Glu1749Val
|
|
NM_001363528.1:c.5216A>T
|
NP_001350457.1:p.Glu1739Val
|
|
NM_021055.2:c.5285A>T
|
NP_066399.2:p.Glu1762Val
|
|
XM_005255531.4:c.5216A>T
|
XP_005255588.2:p.Glu1739Val
|
|
XM_011522636.2:c.5468A>T
|
XP_011520938.1:p.Glu1823Val
|
|
XM_011522637.2:c.5465A>T
|
XP_011520939.1:p.Glu1822Val
|
|
XM_011522638.2:c.5630A>T
|
XP_011520940.2:p.Glu1877Val
|
|
XM_011522639.2:c.5339A>T
|
XP_011520941.1:p.Glu1780Val
|
|
XM_011522640.2:c.5336A>T
|
XP_011520942.1:p.Glu1779Val
|
|
XM_017023615.1:c.5411A>T
|
XP_016879104.1:p.Glu1804Val
|
|
XM_017023616.1:c.5282A>T
|
XP_016879105.1:p.Glu1761Val
|
|
XM_017023617.1:c.5378A>T
|
XP_016879106.1:p.Glu1793Val
|
|
XM_017023618.1:c.4124A>T
|
XP_016879107.1:p.Glu1375Val
|
|
XM_024450413.1:c.5300A>T
|
XP_024306181.1:p.Glu1767Val
|
|
NM_000548.5:c.5414A>T
MANE Select
|
NP_000539.2:p.Glu1805Val
|
|
NM_001370404.1:c.5282A>T
|
NP_001357333.1:p.Glu1761Val
|
|
NM_001370405.1:c.5273A>T
|
NP_001357334.1:p.Glu1758Val
|
|
NM_001077183.3:c.5213A>T
|
NP_001070651.1:p.Glu1738Val
|
|
NM_001114382.3:c.5345A>T
|
NP_001107854.1:p.Glu1782Val
|
|
NM_001318827.2:c.5105A>T
|
NP_001305756.1:p.Glu1702Val
|
|
NM_001318829.2:c.5069A>T
|
NP_001305758.1:p.Glu1690Val
|
|
NM_001318831.2:c.4682A>T
|
NP_001305760.1:p.Glu1561Val
|
|
NM_001318832.2:c.5246A>T
|
NP_001305761.1:p.Glu1749Val
|
|
NM_001363528.2:c.5216A>T
|
NP_001350457.1:p.Glu1739Val
|
|
NM_021055.3:c.5285A>T
|
NP_066399.2:p.Glu1762Val
|
|