ENST00000350026.11:c.3783C=
|
ENSP00000055163.8:p.Gly1261=
|
|
ENST00000414678.8:c.3852C=
|
ENSP00000412835.3:p.Gly1284=
|
|
ENST00000637015.2:c.4071C=
|
ENSP00000489729.2:p.Gly1357=
|
|
ENST00000346085.10:c.3822C=
|
ENSP00000344546.5:p.Gly1274=
|
|
ENST00000350026.10:c.3534C=
|
ENSP00000055163.7:p.Gly1178=
|
|
ENST00000414678.7:c.2100C=
|
ENSP00000412835.2:p.Gly700=
|
|
ENST00000635849.1:c.1263C=
|
ENSP00000490948.1:p.Gly421=
|
|
ENST00000635957.1:c.897C=
|
ENSP00000490385.1:p.Gly299=
|
|
ENST00000636930.2:c.3942C=
MANE Select
|
ENSP00000490491.2:p.Gly1314=
|
|
ENST00000636940.1:n.1939C=
|
|
|
ENST00000637015.1:c.1310C=
|
|
|
ENST00000637568.1:c.1224C=
|
|
|
ENST00000637741.1:n.608C=
|
|
|
ENST00000637810.1:c.1284C=
|
ENSP00000489636.1:p.Gly428=
|
|
ENST00000637904.1:c.1443C=
|
ENSP00000490550.1:p.Gly481=
|
|
ENST00000647938.1:c.3573C=
|
ENSP00000498155.1:p.Gly1191=
|
|
ENST00000346085.9:c.3573C=
|
ENSP00000344546.4:p.Gly1191=
|
|
ENST00000350026.9:c.3534C=
|
ENSP00000055163.7:p.Gly1178=
|
|
ENST00000414678.6:c.2100C=
|
ENSP00000412835.2:p.Gly700=
|
|
NM_017519.2:c.3534C=
|
NP_059989.2:p.Gly1178=
|
|
NM_020732.3:c.3573C=
|
NP_065783.3:p.Gly1191=
|
|
XM_005267069.3:c.3693C=
|
XP_005267126.2:p.Gly1231=
|
|
XM_011535984.1:c.2772C=
|
XP_011534286.1:p.Gly924=
|
|
XM_011535985.1:c.2592C=
|
XP_011534287.1:p.Gly864=
|
|
XM_011535986.1:c.2352C=
|
XP_011534288.1:p.Gly784=
|
|
XM_011535987.1:c.1971C=
|
XP_011534289.1:p.Gly657=
|
|
XM_011535988.1:c.834C=
|
XP_011534290.1:p.Gly278=
|
|
NM_001346813.1:c.3693C=
|
NP_001333742.1:p.Gly1231=
|
|
NM_001363725.1:c.1443C=
|
NP_001350654.1:p.Gly481=
|
|
XM_011535984.2:c.3903C=
|
XP_011534286.2:p.Gly1301=
|
|
XM_011535988.3:c.834C=
|
XP_011534290.1:p.Gly278=
|
|
XM_017011103.2:c.3804C=
|
XP_016866592.1:p.Gly1268=
|
|
XM_017011104.1:c.3774C=
|
XP_016866593.1:p.Gly1258=
|
|
XM_017011105.2:c.3744C=
|
XP_016866594.1:p.Gly1248=
|
|
XM_017011106.2:c.3615C=
|
XP_016866595.1:p.Gly1205=
|
|
XM_017011107.2:c.3594C=
|
XP_016866596.1:p.Gly1198=
|
|
XR_002956289.1:n.3986C=
|
|
|
NM_001363725.2:c.1443C=
|
NP_001350654.1:p.Gly481=
|
|
NM_001371656.1:c.3822C=
|
NP_001358585.1:p.Gly1274=
|
|
NM_001374820.1:c.3822C=
|
NP_001361749.1:p.Gly1274=
|
|
NM_001374828.1:c.3942C=
MANE Select
|
NP_001361757.1:p.Gly1314=
|
|
NM_017519.3:c.3783C=
|
NP_059989.3:p.Gly1261=
|
|