ENST00000350026.11:c.3805G>A
|
ENSP00000055163.8:p.Gly1269Ser
|
|
ENST00000414678.8:c.3874G>A
|
ENSP00000412835.3:p.Gly1292Ser
|
|
ENST00000637015.2:c.4093G>A
|
ENSP00000489729.2:p.Gly1365Ser
|
|
ENST00000346085.10:c.3844G>A
|
ENSP00000344546.5:p.Gly1282Ser
|
|
ENST00000350026.10:c.3556G>A
|
ENSP00000055163.7:p.Gly1186Ser
|
|
ENST00000414678.7:c.2122G>A
|
ENSP00000412835.2:p.Gly708Ser
|
|
ENST00000635849.1:c.1285G>A
|
ENSP00000490948.1:p.Gly429Ser
|
|
ENST00000635957.1:c.919G>A
|
ENSP00000490385.1:p.Gly307Ser
|
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ENST00000636930.2:c.3964G>A
MANE Select
|
ENSP00000490491.2:p.Gly1322Ser
|
|
ENST00000636940.1:n.1961G>A
|
|
|
ENST00000637015.1:c.1332G>A
|
|
|
ENST00000637568.1:c.1246G>A
|
|
|
ENST00000637741.1:n.630G>A
|
|
|
ENST00000637810.1:c.1306G>A
|
ENSP00000489636.1:p.Gly436Ser
|
|
ENST00000637904.1:c.1465G>A
|
ENSP00000490550.1:p.Gly489Ser
|
|
ENST00000647938.1:c.3595G>A
|
ENSP00000498155.1:p.Gly1199Ser
|
|
ENST00000346085.9:c.3595G>A
|
ENSP00000344546.4:p.Gly1199Ser
|
|
ENST00000350026.9:c.3556G>A
|
ENSP00000055163.7:p.Gly1186Ser
|
|
ENST00000414678.6:c.2122G>A
|
ENSP00000412835.2:p.Gly708Ser
|
|
NM_017519.2:c.3556G>A
|
NP_059989.2:p.Gly1186Ser
|
|
NM_020732.3:c.3595G>A
|
NP_065783.3:p.Gly1199Ser
|
|
XM_005267069.3:c.3715G>A
|
XP_005267126.2:p.Gly1239Ser
|
|
XM_011535984.1:c.2794G>A
|
XP_011534286.1:p.Gly932Ser
|
|
XM_011535985.1:c.2614G>A
|
XP_011534287.1:p.Gly872Ser
|
|
XM_011535986.1:c.2374G>A
|
XP_011534288.1:p.Gly792Ser
|
|
XM_011535987.1:c.1993G>A
|
XP_011534289.1:p.Gly665Ser
|
|
XM_011535988.1:c.856G>A
|
XP_011534290.1:p.Gly286Ser
|
|
NM_001346813.1:c.3715G>A
|
NP_001333742.1:p.Gly1239Ser
|
|
NM_001363725.1:c.1465G>A
|
NP_001350654.1:p.Gly489Ser
|
|
XM_011535984.2:c.3925G>A
|
XP_011534286.2:p.Gly1309Ser
|
|
XM_011535988.3:c.856G>A
|
XP_011534290.1:p.Gly286Ser
|
|
XM_017011103.2:c.3826G>A
|
XP_016866592.1:p.Gly1276Ser
|
|
XM_017011104.1:c.3796G>A
|
XP_016866593.1:p.Gly1266Ser
|
|
XM_017011105.2:c.3766G>A
|
XP_016866594.1:p.Gly1256Ser
|
|
XM_017011106.2:c.3637G>A
|
XP_016866595.1:p.Gly1213Ser
|
|
XM_017011107.2:c.3616G>A
|
XP_016866596.1:p.Gly1206Ser
|
|
XR_002956289.1:n.4008G>A
|
|
|
NM_001363725.2:c.1465G>A
|
NP_001350654.1:p.Gly489Ser
|
|
NM_001371656.1:c.3844G>A
|
NP_001358585.1:p.Gly1282Ser
|
|
NM_001374820.1:c.3844G>A
|
NP_001361749.1:p.Gly1282Ser
|
|
NM_001374828.1:c.3964G>A
MANE Select
|
NP_001361757.1:p.Gly1322Ser
|
|
NM_017519.3:c.3805G>A
|
NP_059989.3:p.Gly1269Ser
|
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