ENST00000350026.11:c.3460G>A
|
ENSP00000055163.8:p.Gly1154Ser
|
|
ENST00000414678.8:c.3529G>A
|
ENSP00000412835.3:p.Gly1177Ser
|
|
ENST00000637015.2:c.3748G>A
|
ENSP00000489729.2:p.Gly1250Ser
|
|
ENST00000319584.11:c.1633G>A
|
ENSP00000313006.7:p.Gly545Ser
|
|
ENST00000346085.10:c.3499G>A
|
ENSP00000344546.5:p.Gly1167Ser
|
|
ENST00000350026.10:c.3211G>A
|
ENSP00000055163.7:p.Gly1071Ser
|
|
ENST00000414678.7:c.1777G>A
|
ENSP00000412835.2:p.Gly593Ser
|
|
ENST00000635849.1:c.940G>A
|
ENSP00000490948.1:p.Gly314Ser
|
|
ENST00000635957.1:c.574G>A
|
ENSP00000490385.1:p.Gly192Ser
|
|
ENST00000636930.2:c.3619G>A
MANE Select
|
ENSP00000490491.2:p.Gly1207Ser
|
|
ENST00000636940.1:n.1616G>A
|
|
|
ENST00000637015.1:c.987G>A
|
|
|
ENST00000637568.1:c.901G>A
|
|
|
ENST00000637741.1:n.285G>A
|
|
|
ENST00000637810.1:c.961G>A
|
ENSP00000489636.1:p.Gly321Ser
|
|
ENST00000637904.1:c.1120G>A
|
ENSP00000490550.1:p.Gly374Ser
|
|
ENST00000647938.1:c.3250G>A
|
ENSP00000498155.1:p.Gly1084Ser
|
|
ENST00000319584.10:c.1636G>A
|
ENSP00000313006.6:p.Gly546Ser
|
|
ENST00000346085.9:c.3250G>A
|
ENSP00000344546.4:p.Gly1084Ser
|
|
ENST00000350026.9:c.3211G>A
|
ENSP00000055163.7:p.Gly1071Ser
|
|
ENST00000400790.3:c.412G>A
|
ENSP00000383596.3:p.Gly138Ser
|
|
ENST00000414678.6:c.1777G>A
|
ENSP00000412835.2:p.Gly593Ser
|
|
ENST00000478761.3:c.821G>A
|
|
|
NM_017519.2:c.3211G>A
|
NP_059989.2:p.Gly1071Ser
|
|
NM_020732.3:c.3250G>A
|
NP_065783.3:p.Gly1084Ser
|
|
XM_005267069.3:c.3370G>A
|
XP_005267126.2:p.Gly1124Ser
|
|
XM_011535984.1:c.2449G>A
|
XP_011534286.1:p.Gly817Ser
|
|
XM_011535985.1:c.2269G>A
|
XP_011534287.1:p.Gly757Ser
|
|
XM_011535986.1:c.2029G>A
|
XP_011534288.1:p.Gly677Ser
|
|
XM_011535987.1:c.1648G>A
|
XP_011534289.1:p.Gly550Ser
|
|
XM_011535988.1:c.511G>A
|
XP_011534290.1:p.Gly171Ser
|
|
NM_001346813.1:c.3370G>A
|
NP_001333742.1:p.Gly1124Ser
|
|
NM_001363725.1:c.1120G>A
|
NP_001350654.1:p.Gly374Ser
|
|
XM_011535984.2:c.3580G>A
|
XP_011534286.2:p.Gly1194Ser
|
|
XM_011535988.3:c.511G>A
|
XP_011534290.1:p.Gly171Ser
|
|
XM_017011103.2:c.3481G>A
|
XP_016866592.1:p.Gly1161Ser
|
|
XM_017011104.1:c.3451G>A
|
XP_016866593.1:p.Gly1151Ser
|
|
XM_017011105.2:c.3421G>A
|
XP_016866594.1:p.Gly1141Ser
|
|
XM_017011106.2:c.3292G>A
|
XP_016866595.1:p.Gly1098Ser
|
|
XM_017011107.2:c.3271G>A
|
XP_016866596.1:p.Gly1091Ser
|
|
XR_002956289.1:n.3663G>A
|
|
|
NM_001363725.2:c.1120G>A
|
NP_001350654.1:p.Gly374Ser
|
|
NM_001371656.1:c.3499G>A
|
NP_001358585.1:p.Gly1167Ser
|
|
NM_001374820.1:c.3499G>A
|
NP_001361749.1:p.Gly1167Ser
|
|
NM_001374828.1:c.3619G>A
MANE Select
|
NP_001361757.1:p.Gly1207Ser
|
|
NM_017519.3:c.3460G>A
|
NP_059989.3:p.Gly1154Ser
|
|