|
ENST00000309615.8:c.592G>T
|
ENSP00000311547.4:p.Ala198Ser
|
|
|
ENST00000379817.7:c.754G>T
MANE Select
|
ENSP00000369145.2:p.Ala252Ser
|
|
|
ENST00000379819.6:c.754G>T
|
ENSP00000369147.2:p.Ala252Ser
|
|
|
ENST00000379825.7:c.754G>T
|
ENSP00000369153.3:p.Ala252Ser
|
|
|
ENST00000397172.8:c.538G>T
|
ENSP00000380357.4:p.Ala180Ser
|
|
|
ENST00000436040.7:c.592G>T
|
ENSP00000400806.4:p.Ala198Ser
|
|
|
ENST00000460940.6:c.*388+1324G>T
|
ENSP00000418311.1:n.*388+1324G>T
|
|
|
ENST00000463596.6:c.754G>T
|
ENSP00000419846.1:p.Ala252Ser
|
|
|
ENST00000465003.6:c.*484G>T
|
ENSP00000419430.2:n.*484G>T
|
|
|
ENST00000467331.6:c.*599G>T
|
ENSP00000418733.1:n.*599G>T
|
|
|
ENST00000468275.6:c.754G>T
|
ENSP00000420263.2:p.Ala252Ser
|
|
|
ENST00000472896.6:c.*548G>T
|
ENSP00000417804.2:n.*548G>T
|
|
|
ENST00000474658.7:c.*197G>T
|
ENSP00000417750.3:n.*197G>T
|
|
|
ENST00000476858.6:c.592G>T
|
ENSP00000419042.2:p.Ala198Ser
|
|
|
ENST00000477119.2:c.637G>T
|
ENSP00000417649.2:p.Ala213Ser
|
|
|
ENST00000479656.6:c.*599G>T
|
ENSP00000420071.1:n.*599G>T
|
|
|
ENST00000482687.6:c.*388+1324G>T
|
ENSP00000419289.2:n.*388+1324G>T
|
|
|
ENST00000483148.6:c.*381G>T
|
ENSP00000419723.1:n.*381G>T
|
|
|
ENST00000485479.6:c.*475G>T
|
ENSP00000418144.1:n.*475G>T
|
|
|
ENST00000495360.6:c.*497G>T
|
ENSP00000419623.2:n.*497G>T
|
|
|
ENST00000671774.1:n.352G>T
|
|
|
|
ENST00000671912.1:c.279+1324G>T
|
ENSP00000500871.1:n.279+1324G>T
|
|
|
ENST00000672152.1:n.740+1324G>T
|
|
|
|
ENST00000672244.1:c.381+1324G>T
|
ENSP00000499875.1:n.381+1324G>T
|
|
|
ENST00000672281.1:n.951G>T
|
|
|
|
ENST00000672286.1:n.1015G>T
|
|
|
|
ENST00000672438.1:c.490G>T
|
ENSP00000499997.1:p.Ala164Ser
|
|
|
ENST00000672476.1:n.946G>T
|
|
|
|
ENST00000672493.1:n.1293G>T
|
|
|
|
ENST00000672519.1:c.*388+1324G>T
|
ENSP00000500320.1:n.*388+1324G>T
|
|
|
ENST00000672535.1:c.*484G>T
|
ENSP00000499872.1:n.*484G>T
|
|
|
ENST00000672615.1:n.831G>T
|
|
|
|
ENST00000672846.1:c.*484G>T
|
ENSP00000500396.1:n.*484G>T
|
|
|
ENST00000673114.1:n.618G>T
|
|
|
|
ENST00000673171.1:n.620+1324G>T
|
|
|
|
ENST00000673211.1:n.836G>T
|
|
|
|
ENST00000673248.1:c.490G>T
|
ENSP00000500601.1:p.Ala164Ser
|
|
|
ENST00000673333.1:n.1032G>T
|
|
|
|
ENST00000673360.1:c.*197G>T
|
ENSP00000500360.1:n.*197G>T
|
|
|
ENST00000673416.1:c.490G>T
|
ENSP00000500738.1:p.Ala164Ser
|
|
|
ENST00000673485.1:n.951G>T
|
|
|
|
ENST00000673487.1:c.*484G>T
|
ENSP00000500943.1:n.*484G>T
|
|
|
ENST00000673598.1:c.232G>T
|
ENSP00000499991.1:p.Ala78Ser
|
|
|
ENST00000309615.7:c.592G>T
|
ENSP00000311547.4:p.Ala198Ser
|
|
|
ENST00000379812.9:c.580G>T
|
ENSP00000369140.5:p.Ala194Ser
|
|
|
ENST00000379813.7:c.736G>T
|
ENSP00000369141.4:p.Ala246Ser
|
|
|
ENST00000379817.6:c.754G>T
|
ENSP00000369145.2:p.Ala252Ser
|
|
|
ENST00000379819.5:c.796G>T
|
ENSP00000369147.1:p.Ala266Ser
|
|
|
ENST00000379825.6:c.796G>T
|
ENSP00000369153.2:p.Ala266Ser
|
|
|
ENST00000397172.7:c.580G>T
|
ENSP00000380357.3:p.Ala194Ser
|
|
|
ENST00000436040.6:c.754G>T
|
ENSP00000400806.3:p.Ala252Ser
|
|
|
ENST00000460940.5:c.*388+1324G>T
|
ENSP00000418311.1:n.*388+1324G>T
|
|
|
ENST00000463596.5:c.754G>T
|
ENSP00000419846.1:p.Ala252Ser
|
|
|
ENST00000465003.5:c.*381G>T
|
ENSP00000419430.1:n.*381G>T
|
|
|
ENST00000467331.5:c.*599G>T
|
ENSP00000418733.1:n.*599G>T
|
|
|
ENST00000468275.5:c.754G>T
|
ENSP00000420263.1:p.Ala252Ser
|
|
|
ENST00000472896.5:c.*273+1324G>T
|
ENSP00000417804.1:n.*273+1324G>T
|
|
|
ENST00000473221.5:c.634G>T
|
ENSP00000419020.1:p.Ala212Ser
|
|
|
ENST00000474658.6:c.421G>T
|
|
|
|
ENST00000476858.5:c.634G>T
|
ENSP00000419042.1:p.Ala212Ser
|
|
|
ENST00000479656.5:c.*599G>T
|
ENSP00000420071.1:n.*599G>T
|
|
|
ENST00000482687.5:c.543+1324G>T
|
ENSP00000419289.1:n.543+1324G>T
|
|
|
ENST00000483148.5:c.*170+1324G>T
|
ENSP00000419723.1:n.*170+1324G>T
|
|
|
ENST00000485479.5:c.*484G>T
|
ENSP00000418144.1:n.*484G>T
|
|
|
ENST00000486724.5:n.490G>T
|
|
|
|
ENST00000494649.5:c.*599G>T
|
ENSP00000417634.1:n.*599G>T
|
|
|
ENST00000495360.5:c.*484G>T
|
ENSP00000419623.1:n.*484G>T
|
|
|
NM_001195248.1:c.796G>T
|
NP_001182177.1:p.Ala266Ser
|
|
|
NM_001195249.1:c.754G>T
|
NP_001182178.1:p.Ala252Ser
|
|
|
NM_001195250.1:c.634G>T
|
NP_001182179.1:p.Ala212Ser
|
|
|
NM_001195251.1:c.754G>T
|
NP_001182180.1:p.Ala252Ser
|
|
|
NM_001195252.1:c.580G>T
|
NP_001182181.1:p.Ala194Ser
|
|
|
NM_001195254.1:c.592G>T
|
NP_001182183.1:p.Ala198Ser
|
|
|
NM_175069.2:c.796G>T
|
NP_778239.1:p.Ala266Ser
|
|
|
NM_175073.2:c.754G>T
|
NP_778243.1:p.Ala252Ser
|
|
|
NR_036576.1:n.828G>T
|
|
|
|
NR_036577.1:n.718G>T
|
|
|
|
NR_036578.1:n.850G>T
|
|
|
|
NR_036579.1:n.997G>T
|
|
|
|
XM_006716791.2:c.754G>T
|
XP_006716854.1:p.Ala252Ser
|
|
|
XM_006716792.2:c.490G>T
|
XP_006716855.1:p.Ala164Ser
|
|
|
XM_011517936.1:c.490G>T
|
XP_011516238.1:p.Ala164Ser
|
|
|
XM_011517937.1:c.490G>T
|
XP_011516239.1:p.Ala164Ser
|
|
|
XM_011517938.1:c.490G>T
|
XP_011516240.1:p.Ala164Ser
|
|
|
XM_011517939.1:c.490G>T
|
XP_011516241.1:p.Ala164Ser
|
|
|
XR_428423.2:n.622+1324G>T
|
|
|
|
XR_929276.1:n.833G>T
|
|
|
|
XR_929277.1:n.833G>T
|
|
|
|
XR_929279.1:n.622+1324G>T
|
|
|
|
XM_006716791.4:c.754G>T
|
XP_006716854.1:p.Ala252Ser
|
|
|
XM_006716792.3:c.490G>T
|
XP_006716855.1:p.Ala164Ser
|
|
|
XM_011517938.2:c.490G>T
|
XP_011516240.1:p.Ala164Ser
|
|
|
XM_011517939.3:c.490G>T
|
XP_011516241.1:p.Ala164Ser
|
|
|
XM_017014831.1:c.796G>T
|
XP_016870320.1:p.Ala266Ser
|
|
|
XM_017014832.1:c.796G>T
|
XP_016870321.1:p.Ala266Ser
|
|
|
XM_017014833.2:c.796G>T
|
XP_016870322.1:p.Ala266Ser
|
|
|
XM_017014836.2:c.796G>T
|
XP_016870325.1:p.Ala266Ser
|
|
|
XM_017014837.2:c.592G>T
|
XP_016870326.1:p.Ala198Ser
|
|
|
XM_017014838.1:c.490G>T
|
XP_016870327.1:p.Ala164Ser
|
|
|
XM_024447575.1:c.754G>T
|
XP_024303343.1:p.Ala252Ser
|
|
|
XM_024447576.1:c.754G>T
|
XP_024303344.1:p.Ala252Ser
|
|
|
XM_024447577.1:c.754G>T
|
XP_024303345.1:p.Ala252Ser
|
|
|
XM_024447578.1:c.796G>T
|
XP_024303346.1:p.Ala266Ser
|
|
|
XM_024447579.1:c.754G>T
|
XP_024303347.1:p.Ala252Ser
|
|
|
XM_024447580.1:c.592G>T
|
XP_024303348.1:p.Ala198Ser
|
|
|
XM_024447581.1:c.490G>T
|
XP_024303349.1:p.Ala164Ser
|
|
|
XM_024447582.1:c.490G>T
|
XP_024303350.1:p.Ala164Ser
|
|
|
XR_001746325.2:n.833G>T
|
|
|
|
XR_001746326.2:n.841G>T
|
|
|
|
XR_428423.3:n.622+1324G>T
|
|
|
|
XR_929276.3:n.833G>T
|
|
|
|
XR_929277.3:n.833G>T
|
|
|
|
NM_001195248.2:c.754G>T
MANE Select
|
NP_001182177.2:p.Ala252Ser
|
|
|
NM_001195250.2:c.592G>T
|
NP_001182179.2:p.Ala198Ser
|
|
|
NM_001195252.2:c.538G>T
|
NP_001182181.2:p.Ala180Ser
|
|
|
NM_001368995.1:c.754G>T
|
NP_001355924.1:p.Ala252Ser
|
|
|
NM_001368996.1:c.754G>T
|
NP_001355925.1:p.Ala252Ser
|
|
|
NM_001368997.1:c.754G>T
|
NP_001355926.1:p.Ala252Ser
|
|
|
NM_001368998.1:c.754G>T
|
NP_001355927.1:p.Ala252Ser
|
|
|
NM_001368999.1:c.754G>T
|
NP_001355928.1:p.Ala252Ser
|
|
|
NM_001369000.1:c.592G>T
|
NP_001355929.1:p.Ala198Ser
|
|
|
NM_001369001.1:c.592G>T
|
NP_001355930.1:p.Ala198Ser
|
|
|
NM_001369002.1:c.490G>T
|
NP_001355931.1:p.Ala164Ser
|
|
|
NM_001369003.1:c.490G>T
|
NP_001355932.1:p.Ala164Ser
|
|
|
NM_001369004.1:c.490G>T
|
NP_001355933.1:p.Ala164Ser
|
|
|
NM_001369005.1:c.490G>T
|
NP_001355934.1:p.Ala164Ser
|
|
|
NM_001369006.1:c.490G>T
|
NP_001355935.1:p.Ala164Ser
|
|
|
NM_001370669.1:c.490G>T
|
NP_001357598.1:p.Ala164Ser
|
|
|
NM_001370670.1:c.490G>T
|
NP_001357599.1:p.Ala164Ser
|
|
|
NM_001370673.1:c.490G>T
|
NP_001357602.1:p.Ala164Ser
|
|
|
NM_175069.3:c.754G>T
|
NP_778239.2:p.Ala252Ser
|
|
|
NR_160920.1:n.609+1324G>T
|
|
|
|
NR_160921.1:n.724G>T
|
|
|
|
NR_160922.1:n.955G>T
|
|
|
|
NR_160923.1:n.759G>T
|
|
|
|
NR_160924.1:n.764G>T
|
|
|
|
NR_160925.1:n.960G>T
|
|
|
|
NR_160926.1:n.750G>T
|
|
|
|
NR_160927.1:n.859+1324G>T
|
|
|
|
NR_160928.1:n.749+1324G>T
|
|
|
|
NR_160929.1:n.663+1324G>T
|
|
|
|
NR_160930.1:n.700G>T
|
|
|
|
NR_160931.1:n.939G>T
|
|
|
|
NM_001195249.2:c.754G>T
|
NP_001182178.1:p.Ala252Ser
|
|
|
NM_001195251.2:c.754G>T
|
NP_001182180.1:p.Ala252Ser
|
|
|
NM_001195254.2:c.592G>T
|
NP_001182183.1:p.Ala198Ser
|
|
|
NM_175073.3:c.754G>T
|
NP_778243.1:p.Ala252Ser
|
|
|
NR_036577.2:n.705G>T
|
|
|
