ENST00000350026.11:c.3897A>T
|
ENSP00000055163.8:p.Gly1299=
|
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ENST00000414678.8:c.3966A>T
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ENSP00000412835.3:p.Gly1322=
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ENST00000637015.2:c.4185A>T
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ENSP00000489729.2:p.Gly1395=
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ENST00000346085.10:c.3936A>T
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ENSP00000344546.5:p.Gly1312=
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ENST00000350026.10:c.3648A>T
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ENSP00000055163.7:p.Gly1216=
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ENST00000414678.7:c.2214A>T
|
ENSP00000412835.2:p.Gly738=
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ENST00000635849.1:c.1377A>T
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ENSP00000490948.1:p.Gly459=
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ENST00000635957.1:c.1011A>T
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ENSP00000490385.1:p.Gly337=
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ENST00000636930.2:c.4056A>T
MANE Select
|
ENSP00000490491.2:p.Gly1352=
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ENST00000636940.1:n.2053A>T
|
|
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ENST00000637015.1:c.1424A>T
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|
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ENST00000637568.1:c.1338A>T
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|
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ENST00000637741.1:n.722A>T
|
|
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ENST00000637810.1:c.1398A>T
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ENSP00000489636.1:p.Gly466=
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|
ENST00000637904.1:c.1557A>T
|
ENSP00000490550.1:p.Gly519=
|
|
ENST00000647938.1:c.3687A>T
|
ENSP00000498155.1:p.Gly1229=
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ENST00000346085.9:c.3687A>T
|
ENSP00000344546.4:p.Gly1229=
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|
ENST00000350026.9:c.3648A>T
|
ENSP00000055163.7:p.Gly1216=
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|
ENST00000414678.6:c.2214A>T
|
ENSP00000412835.2:p.Gly738=
|
|
NM_017519.2:c.3648A>T
|
NP_059989.2:p.Gly1216=
|
|
NM_020732.3:c.3687A>T
|
NP_065783.3:p.Gly1229=
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|
XM_005267069.3:c.3807A>T
|
XP_005267126.2:p.Gly1269=
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|
XM_011535984.1:c.2886A>T
|
XP_011534286.1:p.Gly962=
|
|
XM_011535985.1:c.2706A>T
|
XP_011534287.1:p.Gly902=
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|
XM_011535986.1:c.2466A>T
|
XP_011534288.1:p.Gly822=
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XM_011535987.1:c.2085A>T
|
XP_011534289.1:p.Gly695=
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|
XM_011535988.1:c.948A>T
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XP_011534290.1:p.Gly316=
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|
NM_001346813.1:c.3807A>T
|
NP_001333742.1:p.Gly1269=
|
|
NM_001363725.1:c.1557A>T
|
NP_001350654.1:p.Gly519=
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|
XM_011535984.2:c.4017A>T
|
XP_011534286.2:p.Gly1339=
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|
XM_011535988.3:c.948A>T
|
XP_011534290.1:p.Gly316=
|
|
XM_017011103.2:c.3918A>T
|
XP_016866592.1:p.Gly1306=
|
|
XM_017011104.1:c.3888A>T
|
XP_016866593.1:p.Gly1296=
|
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XM_017011105.2:c.3858A>T
|
XP_016866594.1:p.Gly1286=
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|
XM_017011106.2:c.3729A>T
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XP_016866595.1:p.Gly1243=
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|
XM_017011107.2:c.3708A>T
|
XP_016866596.1:p.Gly1236=
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|
XR_002956289.1:n.4100A>T
|
|
|
NM_001363725.2:c.1557A>T
|
NP_001350654.1:p.Gly519=
|
|
NM_001371656.1:c.3936A>T
|
NP_001358585.1:p.Gly1312=
|
|
NM_001374820.1:c.3936A>T
|
NP_001361749.1:p.Gly1312=
|
|
NM_001374828.1:c.4056A>T
MANE Select
|
NP_001361757.1:p.Gly1352=
|
|
NM_017519.3:c.3897A>T
|
NP_059989.3:p.Gly1299=
|
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