ENST00000321264.9:c.1418G>C
MANE Select
|
ENSP00000315351.4:p.Ser473Thr
|
|
ENST00000321264.8:c.1418G>C
|
ENSP00000315351.4:p.Ser473Thr
|
|
ENST00000400769.6:c.*168G>C
|
ENSP00000383580.2:n.*168G>C
|
|
ENST00000403782.5:c.1016G>C
|
ENSP00000384723.1:p.Ser339Thr
|
|
ENST00000436747.5:c.*2654G>C
|
ENSP00000400212.1:n.*2654G>C
|
|
ENST00000445308.1:c.814G>C
|
|
|
ENST00000468064.5:n.1308G>C
|
|
|
ENST00000470343.5:n.899G>C
|
|
|
ENST00000473126.1:n.617G>C
|
|
|
ENST00000486953.5:n.1242G>C
|
|
|
ENST00000610344.1:c.*262G>C
|
ENSP00000481906.1:n.*262G>C
|
|
NM_001287249.1:c.1016G>C
|
NP_001274178.1:p.Ser339Thr
|
|
NM_152783.4:c.1418G>C
|
NP_689996.4:p.Ser473Thr
|
|
NR_109778.1:n.1340G>C
|
|
|
XM_011511734.1:c.1538G>C
|
XP_011510036.1:p.Ser513Thr
|
|
XM_011511735.1:c.1496G>C
|
XP_011510037.1:p.Ser499Thr
|
|
XM_011511736.1:c.1460G>C
|
XP_011510038.1:p.Ser487Thr
|
|
XM_011511750.1:c.*85G>C
|
XP_011510052.1:n.*85G>C
|
|
XM_011511754.1:c.977G>C
|
XP_011510056.1:p.Ser326Thr
|
|
XM_011511755.1:c.968G>C
|
XP_011510057.1:p.Ser323Thr
|
|
XM_011511756.1:c.965G>C
|
XP_011510058.1:p.Ser322Thr
|
|
XR_923004.1:n.2050G>C
|
|
|
XR_923007.1:n.1760G>C
|
|
|
XR_923011.1:n.1861G>C
|
|
|
NM_001352824.1:c.857G>C
|
NP_001339753.1:p.Ser286Thr
|
|
XM_011511734.2:c.1538G>C
|
XP_011510036.1:p.Ser513Thr
|
|
XM_011511735.2:c.1496G>C
|
XP_011510037.1:p.Ser499Thr
|
|
XM_011511736.2:c.1460G>C
|
XP_011510038.1:p.Ser487Thr
|
|
XM_011511750.3:c.*85G>C
|
XP_011510052.1:n.*85G>C
|
|
XM_011511756.2:c.965G>C
|
XP_011510058.1:p.Ser322Thr
|
|
XM_024453102.1:c.1310G>C
|
XP_024308870.1:p.Ser437Thr
|
|
XR_001738918.2:n.1792G>C
|
|
|
XR_001738919.2:n.1726G>C
|
|
|
XR_923004.3:n.2049G>C
|
|
|
XR_923007.3:n.1759G>C
|
|
|
XR_923011.3:n.1860G>C
|
|
|
NM_152783.5:c.1418G>C
MANE Select
|
NP_689996.4:p.Ser473Thr
|
|
NM_001287249.2:c.1016G>C
|
NP_001274178.1:p.Ser339Thr
|
|
NM_001352824.2:c.857G>C
|
NP_001339753.1:p.Ser286Thr
|
|
NR_109778.2:n.1289G>C
|
|
|