|
ENST00000376285.6:c.863G=
MANE Select
|
ENSP00000365462.1:p.Arg288=
|
|
|
ENST00000636366.1:c.742G=
|
|
|
|
ENST00000636420.1:c.742G=
|
|
|
|
ENST00000636475.1:c.742G=
|
|
|
|
ENST00000637657.1:c.742G=
|
|
|
|
ENST00000647303.1:c.*711G=
|
ENSP00000495663.1:n.*711G=
|
|
|
ENST00000376279.7:c.863G=
|
ENSP00000365456.3:p.Arg288=
|
|
|
ENST00000376285.5:c.863G=
|
ENSP00000365462.1:p.Arg288=
|
|
|
ENST00000376286.8:c.785G=
|
ENSP00000365463.4:p.Arg262=
|
|
|
NM_000282.3:c.863G=
|
NP_000273.2:p.Arg288=
|
|
|
NM_001127692.2:c.785G=
|
NP_001121164.1:p.Arg262=
|
|
|
NM_001178004.1:c.863G=
|
NP_001171475.1:p.Arg288=
|
|
|
XM_005254059.2:c.863G=
|
XP_005254116.1:p.Arg288=
|
|
|
XM_011521093.1:c.863G=
|
XP_011519395.1:p.Arg288=
|
|
|
XR_931615.1:n.964G=
|
|
|
|
XR_931616.1:n.964G=
|
|
|
|
NM_001352605.1:c.863G=
|
NP_001339534.1:p.Arg288=
|
|
|
NM_001352606.1:c.863G=
|
NP_001339535.1:p.Arg288=
|
|
|
NM_001352607.1:c.785G=
|
NP_001339536.1:p.Arg262=
|
|
|
NM_001352608.1:c.785G=
|
NP_001339537.1:p.Arg262=
|
|
|
NM_001352609.1:c.863G=
|
NP_001339538.1:p.Arg288=
|
|
|
NM_001352610.1:c.-83G=
|
NP_001339539.1:n.-83G=
|
|
|
NM_001352611.1:c.-83G=
|
NP_001339540.1:n.-83G=
|
|
|
NM_001352612.1:c.-83G=
|
NP_001339541.1:n.-83G=
|
|
|
NR_148027.1:n.969G=
|
|
|
|
NR_148028.1:n.969G=
|
|
|
|
NR_148029.1:n.891G=
|
|
|
|
NR_148030.1:n.969G=
|
|
|
|
NR_148031.1:n.969G=
|
|
|
|
XM_017020605.1:c.863G=
|
XP_016876094.1:p.Arg288=
|
|
|
XM_017020606.1:c.785G=
|
XP_016876095.1:p.Arg262=
|
|
|
XM_017020607.1:c.764G=
|
XP_016876096.1:p.Arg255=
|
|
|
XM_017020609.1:c.764G=
|
XP_016876098.1:p.Arg255=
|
|
|
XM_017020611.1:c.863G=
|
XP_016876100.1:p.Arg288=
|
|
|
XM_017020612.1:c.863G=
|
XP_016876101.1:p.Arg288=
|
|
|
XM_017020613.1:c.863G=
|
XP_016876102.1:p.Arg288=
|
|
|
XM_017020615.1:c.863G=
|
XP_016876104.1:p.Arg288=
|
|
|
XM_017020616.1:c.863G=
|
XP_016876105.1:p.Arg288=
|
|
|
XR_001749567.1:n.964G=
|
|
|
|
XR_001749568.1:n.964G=
|
|
|
|
XR_001749569.1:n.964G=
|
|
|
|
XR_001749574.1:n.815G=
|
|
|
|
XR_001749576.1:n.964G=
|
|
|
|
XR_001749577.1:n.964G=
|
|
|
|
NM_000282.4:c.863G=
MANE Select
|
NP_000273.2:p.Arg288=
|
|
|
NM_001352605.2:c.863G=
|
NP_001339534.1:p.Arg288=
|
|
|
NM_001352606.2:c.863G=
|
NP_001339535.1:p.Arg288=
|
|
|
NM_001352607.2:c.785G=
|
NP_001339536.1:p.Arg262=
|
|
|
NM_001352608.2:c.785G=
|
NP_001339537.1:p.Arg262=
|
|
|
NM_001352609.2:c.863G=
|
NP_001339538.1:p.Arg288=
|
|
|
NM_001352610.2:c.-83G=
|
NP_001339539.1:n.-83G=
|
|
|
NM_001352611.2:c.-83G=
|
NP_001339540.1:n.-83G=
|
|
|
NM_001352612.2:c.-83G=
|
NP_001339541.1:n.-83G=
|
|
|
NR_148027.2:n.891G=
|
|
|
|
NR_148028.2:n.891G=
|
|
|
|
NR_148029.2:n.813G=
|
|
|
|
NR_148030.2:n.891G=
|
|
|
|
NR_148031.2:n.891G=
|
|
|
|
NM_001127692.3:c.785G=
|
NP_001121164.1:p.Arg262=
|
|
|
NM_001178004.2:c.863G=
|
NP_001171475.1:p.Arg288=
|
|
