|
NM_003119.4:c.1948G>T
MANE Select
|
NP_003110.1:p.Asp650Tyr
|
|
ENST00000645818.2:c.1948G>T
MANE Select
|
ENSP00000495795.2:p.Asp650Tyr
|
|
NM_001363850.1:c.1948G>T
|
NP_001350779.1:p.Asp650Tyr
|
|
NM_003119.3:c.1948G>T
|
NP_003110.1:p.Asp650Tyr
|
|
ENST00000268704.6:c.1948G>T
|
ENSP00000268704.2:p.Asp650Tyr
|
|
ENST00000268704.7:c.1927G>T
|
ENSP00000268704.3:p.Asp643Tyr
|
|
ENST00000561702.5:n.933G>T
|
|
|
ENST00000561702.6:n.2620G>T
|
|
|
ENST00000561911.5:c.548G>T
|
ENSP00000457387.1:p.Arg183Leu
|
|
ENST00000566682.1:c.84G>T
|
|
|
ENST00000566682.2:c.989G>T
|
ENSP00000461979.2:p.Arg330Leu
|
|
ENST00000569720.1:n.139G>T
|
|
|
ENST00000569720.2:n.631G>T
|
|
|
ENST00000569820.5:c.1190G>T
|
|
|
ENST00000569820.6:c.2221G>T
|
|
|
ENST00000620811.4:c.711G>T
|
ENSP00000478030.1:p.Thr237=
|
|
ENST00000642226.1:n.2011G>T
|
|
|
ENST00000642334.1:c.3366G>T
|
|
|
ENST00000642814.1:n.1363G>T
|
|
|
ENST00000642984.1:n.1671G>T
|
|
|
ENST00000643105.1:c.2654G>T
|
|
|
ENST00000643350.1:n.1362G>T
|
|
|
ENST00000643409.1:n.2373G>T
|
|
|
ENST00000643496.1:n.1765G>T
|
|
|
ENST00000643649.1:c.1837G>T
|
ENSP00000494806.1:p.Asp613Tyr
|
|
ENST00000643668.1:c.*2242G>T
|
ENSP00000494903.1:n.*2242G>T
|
|
ENST00000643724.1:c.*996G>T
|
ENSP00000496335.1:n.*996G>T
|
|
ENST00000643954.1:c.2847G>T
|
|
|
ENST00000644171.1:n.2708G>T
|
|
|
ENST00000644210.1:c.*520G>T
|
ENSP00000495675.1:n.*520G>T
|
|
ENST00000644225.1:n.1965G>T
|
|
|
ENST00000644281.1:n.2632G>T
|
|
|
ENST00000644464.1:n.601G>T
|
|
|
ENST00000644498.1:c.*1767G>T
|
ENSP00000496244.1:n.*1767G>T
|
|
ENST00000644671.1:c.1605G>T
|
|
|
ENST00000644751.1:c.1136G>T
|
|
|
ENST00000644781.1:c.1903G>T
|
ENSP00000495473.1:p.Asp635Tyr
|
|
ENST00000644901.1:c.*2342G>T
|
ENSP00000493797.1:n.*2342G>T
|
|
ENST00000645042.1:c.*722G>T
|
ENSP00000493908.1:n.*722G>T
|
|
ENST00000645063.1:c.1948G>T
|
ENSP00000493590.1:p.Asp650Tyr
|
|
ENST00000645354.1:c.2708G>T
|
|
|
ENST00000645392.1:n.2289G>T
|
|
|
ENST00000645742.1:n.582G>T
|
|
|
ENST00000645842.1:n.1793G>T
|
|
|
ENST00000645886.1:c.1453G>T
|
|
|
ENST00000645897.1:c.1486G>T
|
ENSP00000495293.1:p.Asp496Tyr
|
|
ENST00000645952.1:n.1813G>T
|
|
|
ENST00000645977.1:n.3066G>T
|
|
|
ENST00000646005.1:n.1706G>T
|
|
|
ENST00000646263.1:c.*821G>T
|
ENSP00000494119.1:n.*821G>T
|
|
ENST00000646303.1:c.1816G>T
|
ENSP00000494160.1:p.Asp606Tyr
|
|
ENST00000646399.1:c.2842G>T
|
|
|
ENST00000646445.1:c.806G>T
|
|
|
ENST00000646531.1:c.*571G>T
|
ENSP00000495185.1:n.*571G>T
|
|
ENST00000646589.1:c.*1076G>T
|
ENSP00000494739.1:n.*1076G>T
|
|
ENST00000646716.1:c.1000G>T
|
ENSP00000495593.1:p.Asp334Tyr
|
|
ENST00000646826.1:c.*621G>T
|
ENSP00000495123.1:n.*621G>T
|
|
ENST00000646930.1:c.*1877G>T
|
ENSP00000495219.1:n.*1877G>T
|
|
ENST00000647032.1:c.1563G>T
|
|
|
ENST00000647079.1:c.1540G>T
|
ENSP00000495967.1:p.Asp514Tyr
|
|
ENST00000647123.1:n.1905G>T
|
|
|
ENST00000647227.1:c.1586G>T
|
|
|
ENST00000647302.1:n.2598G>T
|
|
|
ENST00000647476.1:n.835G>T
|
|
|
ENST00000647491.1:n.1692G>T
|
|
|
XM_006721264.2:c.1948G>T
|
XP_006721327.1:p.Asp650Tyr
|
|
XM_006721264.4:c.1948G>T
|
XP_006721327.1:p.Asp650Tyr
|
|
XR_001751971.2:n.2297G>T
|
|
|
XR_001751972.2:n.3584G>T
|
|
