ENST00000281620.11:c.277A>G
|
ENSP00000281620.7:p.Arg93Gly
|
|
ENST00000682472.1:c.277A>G
|
ENSP00000508103.1:p.Arg93Gly
|
|
ENST00000682580.1:n.229A>G
|
|
|
ENST00000682942.1:n.718A>G
|
|
|
ENST00000682943.1:c.222-2218A>G
|
ENSP00000507323.1:n.222-2218A>G
|
|
ENST00000683303.1:c.277A>G
|
ENSP00000508339.1:p.Arg93Gly
|
|
ENST00000683845.1:n.717A>G
|
|
|
ENST00000683945.1:n.189A>G
|
|
|
ENST00000683960.1:c.277A>G
|
ENSP00000506846.1:p.Arg93Gly
|
|
ENST00000684025.1:n.342A>G
|
|
|
ENST00000684283.1:c.277A>G
|
ENSP00000507994.1:p.Arg93Gly
|
|
ENST00000684424.1:c.157A>G
|
ENSP00000507489.1:p.Arg53Gly
|
|
ENST00000381655.7:c.277A>G
MANE Select
|
ENSP00000371070.2:p.Arg93Gly
|
|
ENST00000255283.9:c.157A>G
|
ENSP00000255283.9:p.Arg53Gly
|
|
ENST00000281620.10:c.-194A>G
|
ENSP00000281620.6:n.-194A>G
|
|
ENST00000381648.7:n.201A>G
|
|
|
ENST00000381655.6:c.277A>G
|
ENSP00000371070.2:p.Arg93Gly
|
|
NM_001313741.1:c.157A>G
|
NP_001300670.1:p.Arg53Gly
|
|
NM_016529.4:c.277A>G
|
NP_057613.4:p.Arg93Gly
|
|
NM_016529.5:c.277A>G
|
NP_057613.4:p.Arg93Gly
|
|
XM_005266419.1:c.157A>G
|
XP_005266476.1:p.Arg53Gly
|
|
XM_011535103.1:c.277A>G
|
XP_011533405.1:p.Arg93Gly
|
|
XM_011535104.1:c.157A>G
|
XP_011533406.1:p.Arg53Gly
|
|
XM_011535106.1:c.277A>G
|
XP_011533408.1:p.Arg93Gly
|
|
XM_011535107.1:c.277A>G
|
XP_011533409.1:p.Arg93Gly
|
|
XM_011535108.1:c.-204A>G
|
XP_011533410.1:n.-204A>G
|
|
XM_011535109.1:c.-204A>G
|
XP_011533411.1:n.-204A>G
|
|
XM_011535110.1:c.-199A>G
|
XP_011533412.1:n.-199A>G
|
|
XM_011535111.1:c.-199A>G
|
XP_011533413.1:n.-199A>G
|
|
XM_011535112.1:c.-204A>G
|
XP_011533414.1:n.-204A>G
|
|
XM_011535113.1:c.277A>G
|
XP_011533415.1:p.Arg93Gly
|
|
XM_011535114.1:c.277A>G
|
XP_011533416.1:p.Arg93Gly
|
|
XM_011535104.3:c.157A>G
|
XP_011533406.1:p.Arg53Gly
|
|
XM_011535107.3:c.277A>G
|
XP_011533409.1:p.Arg93Gly
|
|
XM_011535109.3:c.-204A>G
|
XP_011533411.1:n.-204A>G
|
|
XM_011535113.2:c.277A>G
|
XP_011533415.1:p.Arg93Gly
|
|
XM_017020625.2:c.277A>G
|
XP_016876114.1:p.Arg93Gly
|
|
XM_017020626.1:c.277A>G
|
XP_016876115.1:p.Arg93Gly
|
|
NM_016529.6:c.277A>G
MANE Select
|
NP_057613.4:p.Arg93Gly
|
|