ENST00000350026.11:c.3873C>A
|
ENSP00000055163.8:p.Gly1291=
|
|
ENST00000414678.8:c.3942C>A
|
ENSP00000412835.3:p.Gly1314=
|
|
ENST00000637015.2:c.4161C>A
|
ENSP00000489729.2:p.Gly1387=
|
|
ENST00000346085.10:c.3912C>A
|
ENSP00000344546.5:p.Gly1304=
|
|
ENST00000350026.10:c.3624C>A
|
ENSP00000055163.7:p.Gly1208=
|
|
ENST00000414678.7:c.2190C>A
|
ENSP00000412835.2:p.Gly730=
|
|
ENST00000635849.1:c.1353C>A
|
ENSP00000490948.1:p.Gly451=
|
|
ENST00000635957.1:c.987C>A
|
ENSP00000490385.1:p.Gly329=
|
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ENST00000636930.2:c.4032C>A
MANE Select
|
ENSP00000490491.2:p.Gly1344=
|
|
ENST00000636940.1:n.2029C>A
|
|
|
ENST00000637015.1:c.1400C>A
|
|
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ENST00000637568.1:c.1314C>A
|
|
|
ENST00000637741.1:n.698C>A
|
|
|
ENST00000637810.1:c.1374C>A
|
ENSP00000489636.1:p.Gly458=
|
|
ENST00000637904.1:c.1533C>A
|
ENSP00000490550.1:p.Gly511=
|
|
ENST00000647938.1:c.3663C>A
|
ENSP00000498155.1:p.Gly1221=
|
|
ENST00000346085.9:c.3663C>A
|
ENSP00000344546.4:p.Gly1221=
|
|
ENST00000350026.9:c.3624C>A
|
ENSP00000055163.7:p.Gly1208=
|
|
ENST00000414678.6:c.2190C>A
|
ENSP00000412835.2:p.Gly730=
|
|
NM_017519.2:c.3624C>A
|
NP_059989.2:p.Gly1208=
|
|
NM_020732.3:c.3663C>A
|
NP_065783.3:p.Gly1221=
|
|
XM_005267069.3:c.3783C>A
|
XP_005267126.2:p.Gly1261=
|
|
XM_011535984.1:c.2862C>A
|
XP_011534286.1:p.Gly954=
|
|
XM_011535985.1:c.2682C>A
|
XP_011534287.1:p.Gly894=
|
|
XM_011535986.1:c.2442C>A
|
XP_011534288.1:p.Gly814=
|
|
XM_011535987.1:c.2061C>A
|
XP_011534289.1:p.Gly687=
|
|
XM_011535988.1:c.924C>A
|
XP_011534290.1:p.Gly308=
|
|
NM_001346813.1:c.3783C>A
|
NP_001333742.1:p.Gly1261=
|
|
NM_001363725.1:c.1533C>A
|
NP_001350654.1:p.Gly511=
|
|
XM_011535984.2:c.3993C>A
|
XP_011534286.2:p.Gly1331=
|
|
XM_011535988.3:c.924C>A
|
XP_011534290.1:p.Gly308=
|
|
XM_017011103.2:c.3894C>A
|
XP_016866592.1:p.Gly1298=
|
|
XM_017011104.1:c.3864C>A
|
XP_016866593.1:p.Gly1288=
|
|
XM_017011105.2:c.3834C>A
|
XP_016866594.1:p.Gly1278=
|
|
XM_017011106.2:c.3705C>A
|
XP_016866595.1:p.Gly1235=
|
|
XM_017011107.2:c.3684C>A
|
XP_016866596.1:p.Gly1228=
|
|
XR_002956289.1:n.4076C>A
|
|
|
NM_001363725.2:c.1533C>A
|
NP_001350654.1:p.Gly511=
|
|
NM_001371656.1:c.3912C>A
|
NP_001358585.1:p.Gly1304=
|
|
NM_001374820.1:c.3912C>A
|
NP_001361749.1:p.Gly1304=
|
|
NM_001374828.1:c.4032C>A
MANE Select
|
NP_001361757.1:p.Gly1344=
|
|
NM_017519.3:c.3873C>A
|
NP_059989.3:p.Gly1291=
|
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