ENST00000350026.11:c.3781G>A
|
ENSP00000055163.8:p.Gly1261Ser
|
|
ENST00000414678.8:c.3850G>A
|
ENSP00000412835.3:p.Gly1284Ser
|
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ENST00000637015.2:c.4069G>A
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ENSP00000489729.2:p.Gly1357Ser
|
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ENST00000346085.10:c.3820G>A
|
ENSP00000344546.5:p.Gly1274Ser
|
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ENST00000350026.10:c.3532G>A
|
ENSP00000055163.7:p.Gly1178Ser
|
|
ENST00000414678.7:c.2098G>A
|
ENSP00000412835.2:p.Gly700Ser
|
|
ENST00000635849.1:c.1261G>A
|
ENSP00000490948.1:p.Gly421Ser
|
|
ENST00000635957.1:c.895G>A
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ENSP00000490385.1:p.Gly299Ser
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ENST00000636930.2:c.3940G>A
MANE Select
|
ENSP00000490491.2:p.Gly1314Ser
|
|
ENST00000636940.1:n.1937G>A
|
|
|
ENST00000637015.1:c.1308G>A
|
|
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ENST00000637568.1:c.1222G>A
|
|
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ENST00000637741.1:n.606G>A
|
|
|
ENST00000637810.1:c.1282G>A
|
ENSP00000489636.1:p.Gly428Ser
|
|
ENST00000637904.1:c.1441G>A
|
ENSP00000490550.1:p.Gly481Ser
|
|
ENST00000647938.1:c.3571G>A
|
ENSP00000498155.1:p.Gly1191Ser
|
|
ENST00000346085.9:c.3571G>A
|
ENSP00000344546.4:p.Gly1191Ser
|
|
ENST00000350026.9:c.3532G>A
|
ENSP00000055163.7:p.Gly1178Ser
|
|
ENST00000414678.6:c.2098G>A
|
ENSP00000412835.2:p.Gly700Ser
|
|
NM_017519.2:c.3532G>A
|
NP_059989.2:p.Gly1178Ser
|
|
NM_020732.3:c.3571G>A
|
NP_065783.3:p.Gly1191Ser
|
|
XM_005267069.3:c.3691G>A
|
XP_005267126.2:p.Gly1231Ser
|
|
XM_011535984.1:c.2770G>A
|
XP_011534286.1:p.Gly924Ser
|
|
XM_011535985.1:c.2590G>A
|
XP_011534287.1:p.Gly864Ser
|
|
XM_011535986.1:c.2350G>A
|
XP_011534288.1:p.Gly784Ser
|
|
XM_011535987.1:c.1969G>A
|
XP_011534289.1:p.Gly657Ser
|
|
XM_011535988.1:c.832G>A
|
XP_011534290.1:p.Gly278Ser
|
|
NM_001346813.1:c.3691G>A
|
NP_001333742.1:p.Gly1231Ser
|
|
NM_001363725.1:c.1441G>A
|
NP_001350654.1:p.Gly481Ser
|
|
XM_011535984.2:c.3901G>A
|
XP_011534286.2:p.Gly1301Ser
|
|
XM_011535988.3:c.832G>A
|
XP_011534290.1:p.Gly278Ser
|
|
XM_017011103.2:c.3802G>A
|
XP_016866592.1:p.Gly1268Ser
|
|
XM_017011104.1:c.3772G>A
|
XP_016866593.1:p.Gly1258Ser
|
|
XM_017011105.2:c.3742G>A
|
XP_016866594.1:p.Gly1248Ser
|
|
XM_017011106.2:c.3613G>A
|
XP_016866595.1:p.Gly1205Ser
|
|
XM_017011107.2:c.3592G>A
|
XP_016866596.1:p.Gly1198Ser
|
|
XR_002956289.1:n.3984G>A
|
|
|
NM_001363725.2:c.1441G>A
|
NP_001350654.1:p.Gly481Ser
|
|
NM_001371656.1:c.3820G>A
|
NP_001358585.1:p.Gly1274Ser
|
|
NM_001374820.1:c.3820G>A
|
NP_001361749.1:p.Gly1274Ser
|
|
NM_001374828.1:c.3940G>A
MANE Select
|
NP_001361757.1:p.Gly1314Ser
|
|
NM_017519.3:c.3781G>A
|
NP_059989.3:p.Gly1261Ser
|
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