ENST00000350026.11:c.3806G>T
|
ENSP00000055163.8:p.Gly1269Val
|
|
ENST00000414678.8:c.3875G>T
|
ENSP00000412835.3:p.Gly1292Val
|
|
ENST00000637015.2:c.4094G>T
|
ENSP00000489729.2:p.Gly1365Val
|
|
ENST00000346085.10:c.3845G>T
|
ENSP00000344546.5:p.Gly1282Val
|
|
ENST00000350026.10:c.3557G>T
|
ENSP00000055163.7:p.Gly1186Val
|
|
ENST00000414678.7:c.2123G>T
|
ENSP00000412835.2:p.Gly708Val
|
|
ENST00000635849.1:c.1286G>T
|
ENSP00000490948.1:p.Gly429Val
|
|
ENST00000635957.1:c.920G>T
|
ENSP00000490385.1:p.Gly307Val
|
|
ENST00000636930.2:c.3965G>T
MANE Select
|
ENSP00000490491.2:p.Gly1322Val
|
|
ENST00000636940.1:n.1962G>T
|
|
|
ENST00000637015.1:c.1333G>T
|
|
|
ENST00000637568.1:c.1247G>T
|
|
|
ENST00000637741.1:n.631G>T
|
|
|
ENST00000637810.1:c.1307G>T
|
ENSP00000489636.1:p.Gly436Val
|
|
ENST00000637904.1:c.1466G>T
|
ENSP00000490550.1:p.Gly489Val
|
|
ENST00000647938.1:c.3596G>T
|
ENSP00000498155.1:p.Gly1199Val
|
|
ENST00000346085.9:c.3596G>T
|
ENSP00000344546.4:p.Gly1199Val
|
|
ENST00000350026.9:c.3557G>T
|
ENSP00000055163.7:p.Gly1186Val
|
|
ENST00000414678.6:c.2123G>T
|
ENSP00000412835.2:p.Gly708Val
|
|
NM_017519.2:c.3557G>T
|
NP_059989.2:p.Gly1186Val
|
|
NM_020732.3:c.3596G>T
|
NP_065783.3:p.Gly1199Val
|
|
XM_005267069.3:c.3716G>T
|
XP_005267126.2:p.Gly1239Val
|
|
XM_011535984.1:c.2795G>T
|
XP_011534286.1:p.Gly932Val
|
|
XM_011535985.1:c.2615G>T
|
XP_011534287.1:p.Gly872Val
|
|
XM_011535986.1:c.2375G>T
|
XP_011534288.1:p.Gly792Val
|
|
XM_011535987.1:c.1994G>T
|
XP_011534289.1:p.Gly665Val
|
|
XM_011535988.1:c.857G>T
|
XP_011534290.1:p.Gly286Val
|
|
NM_001346813.1:c.3716G>T
|
NP_001333742.1:p.Gly1239Val
|
|
NM_001363725.1:c.1466G>T
|
NP_001350654.1:p.Gly489Val
|
|
XM_011535984.2:c.3926G>T
|
XP_011534286.2:p.Gly1309Val
|
|
XM_011535988.3:c.857G>T
|
XP_011534290.1:p.Gly286Val
|
|
XM_017011103.2:c.3827G>T
|
XP_016866592.1:p.Gly1276Val
|
|
XM_017011104.1:c.3797G>T
|
XP_016866593.1:p.Gly1266Val
|
|
XM_017011105.2:c.3767G>T
|
XP_016866594.1:p.Gly1256Val
|
|
XM_017011106.2:c.3638G>T
|
XP_016866595.1:p.Gly1213Val
|
|
XM_017011107.2:c.3617G>T
|
XP_016866596.1:p.Gly1206Val
|
|
XR_002956289.1:n.4009G>T
|
|
|
NM_001363725.2:c.1466G>T
|
NP_001350654.1:p.Gly489Val
|
|
NM_001371656.1:c.3845G>T
|
NP_001358585.1:p.Gly1282Val
|
|
NM_001374820.1:c.3845G>T
|
NP_001361749.1:p.Gly1282Val
|
|
NM_001374828.1:c.3965G>T
MANE Select
|
NP_001361757.1:p.Gly1322Val
|
|
NM_017519.3:c.3806G>T
|
NP_059989.3:p.Gly1269Val
|
|