ENST00000350026.11:c.3770G>T
|
ENSP00000055163.8:p.Gly1257Val
|
|
ENST00000414678.8:c.3839G>T
|
ENSP00000412835.3:p.Gly1280Val
|
|
ENST00000637015.2:c.4058G>T
|
ENSP00000489729.2:p.Gly1353Val
|
|
ENST00000346085.10:c.3809G>T
|
ENSP00000344546.5:p.Gly1270Val
|
|
ENST00000350026.10:c.3521G>T
|
ENSP00000055163.7:p.Gly1174Val
|
|
ENST00000414678.7:c.2087G>T
|
ENSP00000412835.2:p.Gly696Val
|
|
ENST00000635849.1:c.1250G>T
|
ENSP00000490948.1:p.Gly417Val
|
|
ENST00000635957.1:c.884G>T
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ENSP00000490385.1:p.Gly295Val
|
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ENST00000636930.2:c.3929G>T
MANE Select
|
ENSP00000490491.2:p.Gly1310Val
|
|
ENST00000636940.1:n.1926G>T
|
|
|
ENST00000637015.1:c.1297G>T
|
|
|
ENST00000637568.1:c.1211G>T
|
|
|
ENST00000637741.1:n.595G>T
|
|
|
ENST00000637810.1:c.1271G>T
|
ENSP00000489636.1:p.Gly424Val
|
|
ENST00000637904.1:c.1430G>T
|
ENSP00000490550.1:p.Gly477Val
|
|
ENST00000647938.1:c.3560G>T
|
ENSP00000498155.1:p.Gly1187Val
|
|
ENST00000346085.9:c.3560G>T
|
ENSP00000344546.4:p.Gly1187Val
|
|
ENST00000350026.9:c.3521G>T
|
ENSP00000055163.7:p.Gly1174Val
|
|
ENST00000414678.6:c.2087G>T
|
ENSP00000412835.2:p.Gly696Val
|
|
NM_017519.2:c.3521G>T
|
NP_059989.2:p.Gly1174Val
|
|
NM_020732.3:c.3560G>T
|
NP_065783.3:p.Gly1187Val
|
|
XM_005267069.3:c.3680G>T
|
XP_005267126.2:p.Gly1227Val
|
|
XM_011535984.1:c.2759G>T
|
XP_011534286.1:p.Gly920Val
|
|
XM_011535985.1:c.2579G>T
|
XP_011534287.1:p.Gly860Val
|
|
XM_011535986.1:c.2339G>T
|
XP_011534288.1:p.Gly780Val
|
|
XM_011535987.1:c.1958G>T
|
XP_011534289.1:p.Gly653Val
|
|
XM_011535988.1:c.821G>T
|
XP_011534290.1:p.Gly274Val
|
|
NM_001346813.1:c.3680G>T
|
NP_001333742.1:p.Gly1227Val
|
|
NM_001363725.1:c.1430G>T
|
NP_001350654.1:p.Gly477Val
|
|
XM_011535984.2:c.3890G>T
|
XP_011534286.2:p.Gly1297Val
|
|
XM_011535988.3:c.821G>T
|
XP_011534290.1:p.Gly274Val
|
|
XM_017011103.2:c.3791G>T
|
XP_016866592.1:p.Gly1264Val
|
|
XM_017011104.1:c.3761G>T
|
XP_016866593.1:p.Gly1254Val
|
|
XM_017011105.2:c.3731G>T
|
XP_016866594.1:p.Gly1244Val
|
|
XM_017011106.2:c.3602G>T
|
XP_016866595.1:p.Gly1201Val
|
|
XM_017011107.2:c.3581G>T
|
XP_016866596.1:p.Gly1194Val
|
|
XR_002956289.1:n.3973G>T
|
|
|
NM_001363725.2:c.1430G>T
|
NP_001350654.1:p.Gly477Val
|
|
NM_001371656.1:c.3809G>T
|
NP_001358585.1:p.Gly1270Val
|
|
NM_001374820.1:c.3809G>T
|
NP_001361749.1:p.Gly1270Val
|
|
NM_001374828.1:c.3929G>T
MANE Select
|
NP_001361757.1:p.Gly1310Val
|
|
NM_017519.3:c.3770G>T
|
NP_059989.3:p.Gly1257Val
|
|