ENST00000350026.11:c.3832G>T
|
ENSP00000055163.8:p.Gly1278Cys
|
|
ENST00000414678.8:c.3901G>T
|
ENSP00000412835.3:p.Gly1301Cys
|
|
ENST00000637015.2:c.4120G>T
|
ENSP00000489729.2:p.Gly1374Cys
|
|
ENST00000346085.10:c.3871G>T
|
ENSP00000344546.5:p.Gly1291Cys
|
|
ENST00000350026.10:c.3583G>T
|
ENSP00000055163.7:p.Gly1195Cys
|
|
ENST00000414678.7:c.2149G>T
|
ENSP00000412835.2:p.Gly717Cys
|
|
ENST00000635849.1:c.1312G>T
|
ENSP00000490948.1:p.Gly438Cys
|
|
ENST00000635957.1:c.946G>T
|
ENSP00000490385.1:p.Gly316Cys
|
|
ENST00000636930.2:c.3991G>T
MANE Select
|
ENSP00000490491.2:p.Gly1331Cys
|
|
ENST00000636940.1:n.1988G>T
|
|
|
ENST00000637015.1:c.1359G>T
|
|
|
ENST00000637568.1:c.1273G>T
|
|
|
ENST00000637741.1:n.657G>T
|
|
|
ENST00000637810.1:c.1333G>T
|
ENSP00000489636.1:p.Gly445Cys
|
|
ENST00000637904.1:c.1492G>T
|
ENSP00000490550.1:p.Gly498Cys
|
|
ENST00000647938.1:c.3622G>T
|
ENSP00000498155.1:p.Gly1208Cys
|
|
ENST00000346085.9:c.3622G>T
|
ENSP00000344546.4:p.Gly1208Cys
|
|
ENST00000350026.9:c.3583G>T
|
ENSP00000055163.7:p.Gly1195Cys
|
|
ENST00000414678.6:c.2149G>T
|
ENSP00000412835.2:p.Gly717Cys
|
|
NM_017519.2:c.3583G>T
|
NP_059989.2:p.Gly1195Cys
|
|
NM_020732.3:c.3622G>T
|
NP_065783.3:p.Gly1208Cys
|
|
XM_005267069.3:c.3742G>T
|
XP_005267126.2:p.Gly1248Cys
|
|
XM_011535984.1:c.2821G>T
|
XP_011534286.1:p.Gly941Cys
|
|
XM_011535985.1:c.2641G>T
|
XP_011534287.1:p.Gly881Cys
|
|
XM_011535986.1:c.2401G>T
|
XP_011534288.1:p.Gly801Cys
|
|
XM_011535987.1:c.2020G>T
|
XP_011534289.1:p.Gly674Cys
|
|
XM_011535988.1:c.883G>T
|
XP_011534290.1:p.Gly295Cys
|
|
NM_001346813.1:c.3742G>T
|
NP_001333742.1:p.Gly1248Cys
|
|
NM_001363725.1:c.1492G>T
|
NP_001350654.1:p.Gly498Cys
|
|
XM_011535984.2:c.3952G>T
|
XP_011534286.2:p.Gly1318Cys
|
|
XM_011535988.3:c.883G>T
|
XP_011534290.1:p.Gly295Cys
|
|
XM_017011103.2:c.3853G>T
|
XP_016866592.1:p.Gly1285Cys
|
|
XM_017011104.1:c.3823G>T
|
XP_016866593.1:p.Gly1275Cys
|
|
XM_017011105.2:c.3793G>T
|
XP_016866594.1:p.Gly1265Cys
|
|
XM_017011106.2:c.3664G>T
|
XP_016866595.1:p.Gly1222Cys
|
|
XM_017011107.2:c.3643G>T
|
XP_016866596.1:p.Gly1215Cys
|
|
XR_002956289.1:n.4035G>T
|
|
|
NM_001363725.2:c.1492G>T
|
NP_001350654.1:p.Gly498Cys
|
|
NM_001371656.1:c.3871G>T
|
NP_001358585.1:p.Gly1291Cys
|
|
NM_001374820.1:c.3871G>T
|
NP_001361749.1:p.Gly1291Cys
|
|
NM_001374828.1:c.3991G>T
MANE Select
|
NP_001361757.1:p.Gly1331Cys
|
|
NM_017519.3:c.3832G>T
|
NP_059989.3:p.Gly1278Cys
|
|