|
ENST00000649042.2:c.2511A>G
|
ENSP00000497790.2:n.2511A>G
|
|
|
ENST00000649724.2:c.2647A>G
|
ENSP00000497932.2:p.Ile883Val
|
|
|
ENST00000680270.2:c.2500A>G
|
ENSP00000505532.2:p.Ile834Val
|
|
|
ENST00000681056.2:c.2269A>G
|
ENSP00000506234.2:p.Ile757Val
|
|
|
ENST00000368471.8:c.1732A>G
|
ENSP00000357456.3:p.Ile578Val
|
|
|
ENST00000368474.9:c.2617A>G
MANE Select
|
ENSP00000357459.4:p.Ile873Val
|
|
|
ENST00000529168.2:c.2539A>G
|
ENSP00000431794.2:p.Ile847Val
|
|
|
ENST00000647682.2:n.2602A>G
|
|
|
|
ENST00000648231.2:c.1732A>G
|
ENSP00000497555.1:p.Ile578Val
|
|
|
ENST00000648311.1:c.1732A>G
|
ENSP00000498137.1:p.Ile578Val
|
|
|
ENST00000648714.2:c.*92A>G
|
ENSP00000497434.2:n.*92A>G
|
|
|
ENST00000649021.1:n.2653A>G
|
|
|
|
ENST00000649022.2:c.1732A>G
|
ENSP00000496896.2:p.Ile578Val
|
|
|
ENST00000649042.1:c.1732A>G
|
ENSP00000497790.1:p.Ile578Val
|
|
|
ENST00000649408.2:c.2617A>G
|
ENSP00000497386.2:p.Ile873Val
|
|
|
ENST00000649724.1:c.1732A>G
|
ENSP00000497932.1:p.Ile578Val
|
|
|
ENST00000649749.1:c.1732A>G
|
ENSP00000497210.1:p.Ile578Val
|
|
|
ENST00000679375.1:c.*849A>G
|
ENSP00000505887.1:n.*849A>G
|
|
|
ENST00000679465.1:n.3070A>G
|
|
|
|
ENST00000679805.1:n.2653A>G
|
|
|
|
ENST00000679899.1:c.1675A>G
|
ENSP00000505996.1:p.Ile559Val
|
|
|
ENST00000680270.1:c.1732A>G
|
ENSP00000505532.1:p.Ile578Val
|
|
|
ENST00000680305.1:c.2617A>G
|
ENSP00000506312.1:p.Ile873Val
|
|
|
ENST00000681056.1:c.1732A>G
|
ENSP00000506234.1:p.Ile578Val
|
|
|
ENST00000681235.1:c.*2139A>G
|
ENSP00000506606.1:n.*2139A>G
|
|
|
ENST00000681429.1:n.1877A>G
|
|
|
|
ENST00000681683.1:c.1732A>G
|
ENSP00000506666.1:p.Ile578Val
|
|
|
ENST00000681786.1:n.3070A>G
|
|
|
|
ENST00000681901.1:c.*2217A>G
|
ENSP00000504883.1:n.*2217A>G
|
|
|
ENST00000368471.7:c.1732A>G
|
ENSP00000357456.3:p.Ile578Val
|
|
|
ENST00000368474.8:c.2617A>G
|
ENSP00000357459.4:p.Ile873Val
|
|
|
ENST00000529168.1:c.2524A>G
|
ENSP00000431794.1:p.Ile842Val
|
|
|
NM_001025107.2:c.1732A>G
|
NP_001020278.1:p.Ile578Val
|
|
|
NM_001111.4:c.2617A>G
|
NP_001102.2:p.Ile873Val
|
|
|
NM_001193495.1:c.1732A>G
|
NP_001180424.1:p.Ile578Val
|
|
|
NM_015840.3:c.2539A>G
|
NP_056655.2:p.Ile847Val
|
|
|
NM_015841.3:c.2482A>G
|
NP_056656.2:p.Ile828Val
|
|
|
XM_006711109.1:c.2647A>G
|
XP_006711172.1:p.Ile883Val
|
|
|
XM_006711111.2:c.1732A>G
|
XP_006711174.1:p.Ile578Val
|
|
|
XM_006711112.1:c.1732A>G
|
XP_006711175.1:p.Ile578Val
|
|
|
XM_006711113.1:c.1732A>G
|
XP_006711176.1:p.Ile578Val
|
|
|
XM_011509060.1:c.2746A>G
|
XP_011507362.1:p.Ile916Val
|
|
|
XM_011509061.1:c.2668A>G
|
XP_011507363.1:p.Ile890Val
|
|
|
XM_011509062.1:c.2635A>G
|
XP_011507364.1:p.Ile879Val
|
|
|
NM_001025107.3:c.1732A>G
|
NP_001020278.1:p.Ile578Val
|
|
|
NM_001111.5:c.2617A>G
MANE Select
|
NP_001102.3:p.Ile873Val
|
|
|
NM_001193495.2:c.1732A>G
|
NP_001180424.1:p.Ile578Val
|
|
|
NM_001365045.1:c.2644A>G
|
NP_001351974.1:p.Ile882Val
|
|
|
NM_001365046.1:c.1732A>G
|
NP_001351975.1:p.Ile578Val
|
|
|
NM_001365047.1:c.1732A>G
|
NP_001351976.1:p.Ile578Val
|
|
|
NM_001365048.1:c.1732A>G
|
NP_001351977.1:p.Ile578Val
|
|
|
NM_001365049.1:c.1654A>G
|
NP_001351978.1:p.Ile552Val
|
|
|
NM_015840.4:c.2539A>G
|
NP_056655.3:p.Ile847Val
|
|
|
NM_015841.4:c.2482A>G
|
NP_056656.3:p.Ile828Val
|
|
|
XM_006711113.2:c.1732A>G
|
XP_006711176.1:p.Ile578Val
|
|
|
XM_011509061.2:c.1654A>G
|
XP_011507363.2:p.Ile552Val
|
|
|
XM_024449674.1:c.2746A>G
|
XP_024305442.1:p.Ile916Val
|
|
