ENST00000380044.6:c.271T>G
MANE Select
|
ENSP00000369383.1:p.Leu91Val
|
|
ENST00000233545.6:c.271T>G
|
ENSP00000233545.2:p.Leu91Val
|
|
ENST00000357186.10:c.103T>G
|
ENSP00000349713.6:p.Leu35Val
|
|
ENST00000380044.5:c.271T>G
|
ENSP00000369383.1:p.Leu91Val
|
|
ENST00000402310.5:c.271T>G
|
ENSP00000383955.1:p.Leu91Val
|
|
ENST00000402722.5:c.236T>G
|
ENSP00000386000.1:p.Val79Gly
|
|
ENST00000403262.6:c.271T>G
|
ENSP00000385671.1:p.Leu91Val
|
|
ENST00000405076.5:c.186+306T>G
|
ENSP00000385175.1:n.186+306T>G
|
|
ENST00000405983.5:c.316T>G
|
ENSP00000384586.1:p.Leu106Val
|
|
ENST00000415514.5:c.*72T>G
|
ENSP00000388043.1:n.*72T>G
|
|
ENST00000426513.6:c.236T>G
|
ENSP00000403824.2:p.Val79Gly
|
|
ENST00000428910.5:c.193T>G
|
ENSP00000405235.1:p.Leu65Val
|
|
ENST00000430991.5:c.201T>G
|
|
|
ENST00000475085.1:n.299T>G
|
|
|
ENST00000616446.1:n.248T>G
|
|
|
ENST00000616707.1:n.700T>G
|
|
|
ENST00000617583.4:n.297T>G
|
|
|
ENST00000621183.4:n.327T>G
|
|
|
ENST00000621470.4:n.287T>G
|
|
|
ENST00000622003.4:n.444T>G
|
|
|
NM_002437.4:c.271T>G
|
NP_002428.1:p.Leu91Val
|
|
XM_005264326.2:c.271T>G
|
XP_005264383.1:p.Leu91Val
|
|
XM_005264327.2:c.112T>G
|
XP_005264384.1:p.Leu38Val
|
|
XM_006712021.2:c.223T>G
|
XP_006712084.1:p.Leu75Val
|
|
XM_005264326.4:c.271T>G
|
XP_005264383.1:p.Leu91Val
|
|
XM_006712021.3:c.223T>G
|
XP_006712084.1:p.Leu75Val
|
|
XM_017004150.1:c.253T>G
|
XP_016859639.1:p.Leu85Val
|
|
XM_017004151.1:c.223T>G
|
XP_016859640.1:p.Leu75Val
|
|
XM_017004152.1:c.112T>G
|
XP_016859641.1:p.Leu38Val
|
|
XM_024452913.1:c.223T>G
|
XP_024308681.1:p.Leu75Val
|
|
NM_002437.5:c.271T>G
MANE Select
|
NP_002428.1:p.Leu91Val
|
|