ENST00000350026.11:c.3894T>G
|
ENSP00000055163.8:p.Gly1298=
|
|
ENST00000414678.8:c.3963T>G
|
ENSP00000412835.3:p.Gly1321=
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ENST00000637015.2:c.4182T>G
|
ENSP00000489729.2:p.Gly1394=
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|
ENST00000346085.10:c.3933T>G
|
ENSP00000344546.5:p.Gly1311=
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ENST00000350026.10:c.3645T>G
|
ENSP00000055163.7:p.Gly1215=
|
|
ENST00000414678.7:c.2211T>G
|
ENSP00000412835.2:p.Gly737=
|
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ENST00000635849.1:c.1374T>G
|
ENSP00000490948.1:p.Gly458=
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ENST00000635957.1:c.1008T>G
|
ENSP00000490385.1:p.Gly336=
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ENST00000636930.2:c.4053T>G
MANE Select
|
ENSP00000490491.2:p.Gly1351=
|
|
ENST00000636940.1:n.2050T>G
|
|
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ENST00000637015.1:c.1421T>G
|
|
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ENST00000637568.1:c.1335T>G
|
|
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ENST00000637741.1:n.719T>G
|
|
|
ENST00000637810.1:c.1395T>G
|
ENSP00000489636.1:p.Gly465=
|
|
ENST00000637904.1:c.1554T>G
|
ENSP00000490550.1:p.Gly518=
|
|
ENST00000647938.1:c.3684T>G
|
ENSP00000498155.1:p.Gly1228=
|
|
ENST00000346085.9:c.3684T>G
|
ENSP00000344546.4:p.Gly1228=
|
|
ENST00000350026.9:c.3645T>G
|
ENSP00000055163.7:p.Gly1215=
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|
ENST00000414678.6:c.2211T>G
|
ENSP00000412835.2:p.Gly737=
|
|
NM_017519.2:c.3645T>G
|
NP_059989.2:p.Gly1215=
|
|
NM_020732.3:c.3684T>G
|
NP_065783.3:p.Gly1228=
|
|
XM_005267069.3:c.3804T>G
|
XP_005267126.2:p.Gly1268=
|
|
XM_011535984.1:c.2883T>G
|
XP_011534286.1:p.Gly961=
|
|
XM_011535985.1:c.2703T>G
|
XP_011534287.1:p.Gly901=
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|
XM_011535986.1:c.2463T>G
|
XP_011534288.1:p.Gly821=
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|
XM_011535987.1:c.2082T>G
|
XP_011534289.1:p.Gly694=
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|
XM_011535988.1:c.945T>G
|
XP_011534290.1:p.Gly315=
|
|
NM_001346813.1:c.3804T>G
|
NP_001333742.1:p.Gly1268=
|
|
NM_001363725.1:c.1554T>G
|
NP_001350654.1:p.Gly518=
|
|
XM_011535984.2:c.4014T>G
|
XP_011534286.2:p.Gly1338=
|
|
XM_011535988.3:c.945T>G
|
XP_011534290.1:p.Gly315=
|
|
XM_017011103.2:c.3915T>G
|
XP_016866592.1:p.Gly1305=
|
|
XM_017011104.1:c.3885T>G
|
XP_016866593.1:p.Gly1295=
|
|
XM_017011105.2:c.3855T>G
|
XP_016866594.1:p.Gly1285=
|
|
XM_017011106.2:c.3726T>G
|
XP_016866595.1:p.Gly1242=
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|
XM_017011107.2:c.3705T>G
|
XP_016866596.1:p.Gly1235=
|
|
XR_002956289.1:n.4097T>G
|
|
|
NM_001363725.2:c.1554T>G
|
NP_001350654.1:p.Gly518=
|
|
NM_001371656.1:c.3933T>G
|
NP_001358585.1:p.Gly1311=
|
|
NM_001374820.1:c.3933T>G
|
NP_001361749.1:p.Gly1311=
|
|
NM_001374828.1:c.4053T>G
MANE Select
|
NP_001361757.1:p.Gly1351=
|
|
NM_017519.3:c.3894T>G
|
NP_059989.3:p.Gly1298=
|
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