ENST00000350026.11:c.4587G>A
|
ENSP00000055163.8:p.Gly1529=
|
|
ENST00000414678.8:c.4656G>A
|
ENSP00000412835.3:p.Gly1552=
|
|
ENST00000637015.2:c.4875G>A
|
ENSP00000489729.2:p.Gly1625=
|
|
ENST00000346085.10:c.4626G>A
|
ENSP00000344546.5:p.Gly1542=
|
|
ENST00000350026.10:c.4338G>A
|
ENSP00000055163.7:p.Gly1446=
|
|
ENST00000414678.7:c.2904G>A
|
ENSP00000412835.2:p.Gly968=
|
|
ENST00000635849.1:c.2067G>A
|
ENSP00000490948.1:p.Gly689=
|
|
ENST00000635957.1:c.1698G>A
|
ENSP00000490385.1:p.Gly566=
|
|
ENST00000636227.1:n.3209G>A
|
|
|
ENST00000636254.1:n.666G>A
|
|
|
ENST00000636930.2:c.4746G>A
MANE Select
|
ENSP00000490491.2:p.Gly1582=
|
|
ENST00000636940.1:n.2743G>A
|
|
|
ENST00000637015.1:c.2114G>A
|
|
|
ENST00000637568.1:c.2028G>A
|
|
|
ENST00000637741.1:n.1412G>A
|
|
|
ENST00000637810.1:c.2088G>A
|
ENSP00000489636.1:p.Gly696=
|
|
ENST00000637904.1:c.2247G>A
|
ENSP00000490550.1:p.Gly749=
|
|
ENST00000647938.1:c.4377G>A
|
ENSP00000498155.1:p.Gly1459=
|
|
ENST00000346085.9:c.4377G>A
|
ENSP00000344546.4:p.Gly1459=
|
|
ENST00000350026.9:c.4338G>A
|
ENSP00000055163.7:p.Gly1446=
|
|
ENST00000414678.6:c.2904G>A
|
ENSP00000412835.2:p.Gly968=
|
|
NM_017519.2:c.4338G>A
|
NP_059989.2:p.Gly1446=
|
|
NM_020732.3:c.4377G>A
|
NP_065783.3:p.Gly1459=
|
|
XM_005267069.3:c.4497G>A
|
XP_005267126.2:p.Gly1499=
|
|
XM_011535984.1:c.3576G>A
|
XP_011534286.1:p.Gly1192=
|
|
XM_011535985.1:c.3396G>A
|
XP_011534287.1:p.Gly1132=
|
|
XM_011535986.1:c.3156G>A
|
XP_011534288.1:p.Gly1052=
|
|
XM_011535987.1:c.2775G>A
|
XP_011534289.1:p.Gly925=
|
|
XM_011535988.1:c.1638G>A
|
XP_011534290.1:p.Gly546=
|
|
NM_001346813.1:c.4497G>A
|
NP_001333742.1:p.Gly1499=
|
|
NM_001363725.1:c.2247G>A
|
NP_001350654.1:p.Gly749=
|
|
XM_011535984.2:c.4707G>A
|
XP_011534286.2:p.Gly1569=
|
|
XM_011535988.3:c.1638G>A
|
XP_011534290.1:p.Gly546=
|
|
XM_017011103.2:c.4608G>A
|
XP_016866592.1:p.Gly1536=
|
|
XM_017011104.1:c.4578G>A
|
XP_016866593.1:p.Gly1526=
|
|
XM_017011105.2:c.4548G>A
|
XP_016866594.1:p.Gly1516=
|
|
XM_017011106.2:c.4419G>A
|
XP_016866595.1:p.Gly1473=
|
|
XM_017011107.2:c.4398G>A
|
XP_016866596.1:p.Gly1466=
|
|
XR_002956289.1:n.4693G>A
|
|
|
NM_001363725.2:c.2247G>A
|
NP_001350654.1:p.Gly749=
|
|
NM_001371656.1:c.4626G>A
|
NP_001358585.1:p.Gly1542=
|
|
NM_001374820.1:c.4626G>A
|
NP_001361749.1:p.Gly1542=
|
|
NM_001374828.1:c.4746G>A
MANE Select
|
NP_001361757.1:p.Gly1582=
|
|
NM_017519.3:c.4587G>A
|
NP_059989.3:p.Gly1529=
|
|