ENST00000380044.6:c.443T>G
MANE Select
|
ENSP00000369383.1:p.Leu148Arg
|
|
ENST00000233545.6:c.443T>G
|
ENSP00000233545.2:p.Leu148Arg
|
|
ENST00000357186.10:c.275T>G
|
ENSP00000349713.6:p.Leu92Arg
|
|
ENST00000380044.5:c.443T>G
|
ENSP00000369383.1:p.Leu148Arg
|
|
ENST00000402310.5:c.408+297T>G
|
ENSP00000383955.1:n.408+297T>G
|
|
ENST00000402722.5:c.*40+577T>G
|
ENSP00000386000.1:n.*40+577T>G
|
|
ENST00000403262.6:c.443T>G
|
ENSP00000385671.1:p.Leu148Arg
|
|
ENST00000405076.5:c.254T>G
|
ENSP00000385175.1:p.Leu85Arg
|
|
ENST00000405983.5:c.488T>G
|
ENSP00000384586.1:p.Leu163Arg
|
|
ENST00000415514.5:c.*244T>G
|
ENSP00000388043.1:n.*244T>G
|
|
ENST00000426513.6:c.*108T>G
|
ENSP00000403824.2:n.*108T>G
|
|
ENST00000430991.5:c.277T>G
|
|
|
ENST00000616707.1:n.1471T>G
|
|
|
ENST00000620797.4:n.116T>G
|
|
|
ENST00000621183.4:n.746T>G
|
|
|
NM_002437.4:c.443T>G
|
NP_002428.1:p.Leu148Arg
|
|
XM_005264326.2:c.443T>G
|
XP_005264383.1:p.Leu148Arg
|
|
XM_005264327.2:c.284T>G
|
XP_005264384.1:p.Leu95Arg
|
|
XM_006712021.2:c.395T>G
|
XP_006712084.1:p.Leu132Arg
|
|
XM_005264326.4:c.443T>G
|
XP_005264383.1:p.Leu148Arg
|
|
XM_006712021.3:c.395T>G
|
XP_006712084.1:p.Leu132Arg
|
|
XM_017004150.1:c.425T>G
|
XP_016859639.1:p.Leu142Arg
|
|
XM_017004151.1:c.395T>G
|
XP_016859640.1:p.Leu132Arg
|
|
XM_017004152.1:c.284T>G
|
XP_016859641.1:p.Leu95Arg
|
|
XM_024452913.1:c.395T>G
|
XP_024308681.1:p.Leu132Arg
|
|
NM_002437.5:c.443T>G
MANE Select
|
NP_002428.1:p.Leu148Arg
|
|