ENST00000321264.9:c.1391G>C
MANE Select
|
ENSP00000315351.4:p.Trp464Ser
|
|
ENST00000321264.8:c.1391G>C
|
ENSP00000315351.4:p.Trp464Ser
|
|
ENST00000400769.6:c.*141G>C
|
ENSP00000383580.2:n.*141G>C
|
|
ENST00000403782.5:c.989G>C
|
ENSP00000384723.1:p.Trp330Ser
|
|
ENST00000436747.5:c.*2627G>C
|
ENSP00000400212.1:n.*2627G>C
|
|
ENST00000445308.1:c.787G>C
|
|
|
ENST00000468064.5:n.1281G>C
|
|
|
ENST00000470343.5:n.872G>C
|
|
|
ENST00000473126.1:n.590G>C
|
|
|
ENST00000486953.5:n.1215G>C
|
|
|
ENST00000610344.1:c.*235G>C
|
ENSP00000481906.1:n.*235G>C
|
|
NM_001287249.1:c.989G>C
|
NP_001274178.1:p.Trp330Ser
|
|
NM_152783.4:c.1391G>C
|
NP_689996.4:p.Trp464Ser
|
|
NR_109778.1:n.1313G>C
|
|
|
XM_011511734.1:c.1511G>C
|
XP_011510036.1:p.Trp504Ser
|
|
XM_011511735.1:c.1469G>C
|
XP_011510037.1:p.Trp490Ser
|
|
XM_011511736.1:c.1433G>C
|
XP_011510038.1:p.Trp478Ser
|
|
XM_011511744.1:c.*123G>C
|
XP_011510046.1:n.*123G>C
|
|
XM_011511750.1:c.*58G>C
|
XP_011510052.1:n.*58G>C
|
|
XM_011511754.1:c.950G>C
|
XP_011510056.1:p.Trp317Ser
|
|
XM_011511755.1:c.941G>C
|
XP_011510057.1:p.Trp314Ser
|
|
XM_011511756.1:c.938G>C
|
XP_011510058.1:p.Trp313Ser
|
|
XR_923004.1:n.2023G>C
|
|
|
XR_923007.1:n.1733G>C
|
|
|
XR_923011.1:n.1834G>C
|
|
|
NM_001352824.1:c.830G>C
|
NP_001339753.1:p.Trp277Ser
|
|
XM_011511734.2:c.1511G>C
|
XP_011510036.1:p.Trp504Ser
|
|
XM_011511735.2:c.1469G>C
|
XP_011510037.1:p.Trp490Ser
|
|
XM_011511736.2:c.1433G>C
|
XP_011510038.1:p.Trp478Ser
|
|
XM_011511750.3:c.*58G>C
|
XP_011510052.1:n.*58G>C
|
|
XM_011511756.2:c.938G>C
|
XP_011510058.1:p.Trp313Ser
|
|
XM_024453102.1:c.1283G>C
|
XP_024308870.1:p.Trp428Ser
|
|
XR_001738918.2:n.1765G>C
|
|
|
XR_001738919.2:n.1699G>C
|
|
|
XR_923004.3:n.2022G>C
|
|
|
XR_923007.3:n.1732G>C
|
|
|
XR_923011.3:n.1833G>C
|
|
|
NM_152783.5:c.1391G>C
MANE Select
|
NP_689996.4:p.Trp464Ser
|
|
NM_001287249.2:c.989G>C
|
NP_001274178.1:p.Trp330Ser
|
|
NM_001352824.2:c.830G>C
|
NP_001339753.1:p.Trp277Ser
|
|
NR_109778.2:n.1262G>C
|
|
|