ENST00000380044.6:c.269T>C
MANE Select
|
ENSP00000369383.1:p.Leu90Ser
|
|
ENST00000233545.6:c.269T>C
|
ENSP00000233545.2:p.Leu90Ser
|
|
ENST00000357186.10:c.101T>C
|
ENSP00000349713.6:p.Leu34Ser
|
|
ENST00000380044.5:c.269T>C
|
ENSP00000369383.1:p.Leu90Ser
|
|
ENST00000402310.5:c.269T>C
|
ENSP00000383955.1:p.Leu90Ser
|
|
ENST00000402722.5:c.234T>C
|
ENSP00000386000.1:p.Val78=
|
|
ENST00000403262.6:c.269T>C
|
ENSP00000385671.1:p.Leu90Ser
|
|
ENST00000405076.5:c.186+304T>C
|
ENSP00000385175.1:n.186+304T>C
|
|
ENST00000405983.5:c.314T>C
|
ENSP00000384586.1:p.Leu105Ser
|
|
ENST00000415514.5:c.*70T>C
|
ENSP00000388043.1:n.*70T>C
|
|
ENST00000426513.6:c.234T>C
|
ENSP00000403824.2:p.Val78=
|
|
ENST00000428910.5:c.191T>C
|
ENSP00000405235.1:p.Leu64Ser
|
|
ENST00000430991.5:c.199T>C
|
|
|
ENST00000475085.1:n.297T>C
|
|
|
ENST00000616446.1:n.246T>C
|
|
|
ENST00000616707.1:n.698T>C
|
|
|
ENST00000617583.4:n.295T>C
|
|
|
ENST00000621183.4:n.325T>C
|
|
|
ENST00000621470.4:n.285T>C
|
|
|
ENST00000622003.4:n.442T>C
|
|
|
NM_002437.4:c.269T>C
|
NP_002428.1:p.Leu90Ser
|
|
XM_005264326.2:c.269T>C
|
XP_005264383.1:p.Leu90Ser
|
|
XM_005264327.2:c.110T>C
|
XP_005264384.1:p.Leu37Ser
|
|
XM_006712021.2:c.221T>C
|
XP_006712084.1:p.Leu74Ser
|
|
XM_005264326.4:c.269T>C
|
XP_005264383.1:p.Leu90Ser
|
|
XM_006712021.3:c.221T>C
|
XP_006712084.1:p.Leu74Ser
|
|
XM_017004150.1:c.251T>C
|
XP_016859639.1:p.Leu84Ser
|
|
XM_017004151.1:c.221T>C
|
XP_016859640.1:p.Leu74Ser
|
|
XM_017004152.1:c.110T>C
|
XP_016859641.1:p.Leu37Ser
|
|
XM_024452913.1:c.221T>C
|
XP_024308681.1:p.Leu74Ser
|
|
NM_002437.5:c.269T>C
MANE Select
|
NP_002428.1:p.Leu90Ser
|
|