ENST00000350026.11:c.3778C=
|
ENSP00000055163.8:p.Gln1260=
|
|
ENST00000414678.8:c.3847C=
|
ENSP00000412835.3:p.Gln1283=
|
|
ENST00000637015.2:c.4066C=
|
ENSP00000489729.2:p.Gln1356=
|
|
ENST00000346085.10:c.3817C=
|
ENSP00000344546.5:p.Gln1273=
|
|
ENST00000350026.10:c.3529C=
|
ENSP00000055163.7:p.Gln1177=
|
|
ENST00000414678.7:c.2095C=
|
ENSP00000412835.2:p.Gln699=
|
|
ENST00000635849.1:c.1258C=
|
ENSP00000490948.1:p.Gln420=
|
|
ENST00000635957.1:c.892C=
|
ENSP00000490385.1:p.Gln298=
|
|
ENST00000636930.2:c.3937C=
MANE Select
|
ENSP00000490491.2:p.Gln1313=
|
|
ENST00000636940.1:n.1934C=
|
|
|
ENST00000637015.1:c.1305C=
|
|
|
ENST00000637568.1:c.1219C=
|
|
|
ENST00000637741.1:n.603C=
|
|
|
ENST00000637810.1:c.1279C=
|
ENSP00000489636.1:p.Gln427=
|
|
ENST00000637904.1:c.1438C=
|
ENSP00000490550.1:p.Gln480=
|
|
ENST00000647938.1:c.3568C=
|
ENSP00000498155.1:p.Gln1190=
|
|
ENST00000346085.9:c.3568C=
|
ENSP00000344546.4:p.Gln1190=
|
|
ENST00000350026.9:c.3529C=
|
ENSP00000055163.7:p.Gln1177=
|
|
ENST00000414678.6:c.2095C=
|
ENSP00000412835.2:p.Gln699=
|
|
NM_017519.2:c.3529C=
|
NP_059989.2:p.Gln1177=
|
|
NM_020732.3:c.3568C=
|
NP_065783.3:p.Gln1190=
|
|
XM_005267069.3:c.3688C=
|
XP_005267126.2:p.Gln1230=
|
|
XM_011535984.1:c.2767C=
|
XP_011534286.1:p.Gln923=
|
|
XM_011535985.1:c.2587C=
|
XP_011534287.1:p.Gln863=
|
|
XM_011535986.1:c.2347C=
|
XP_011534288.1:p.Gln783=
|
|
XM_011535987.1:c.1966C=
|
XP_011534289.1:p.Gln656=
|
|
XM_011535988.1:c.829C=
|
XP_011534290.1:p.Gln277=
|
|
NM_001346813.1:c.3688C=
|
NP_001333742.1:p.Gln1230=
|
|
NM_001363725.1:c.1438C=
|
NP_001350654.1:p.Gln480=
|
|
XM_011535984.2:c.3898C=
|
XP_011534286.2:p.Gln1300=
|
|
XM_011535988.3:c.829C=
|
XP_011534290.1:p.Gln277=
|
|
XM_017011103.2:c.3799C=
|
XP_016866592.1:p.Gln1267=
|
|
XM_017011104.1:c.3769C=
|
XP_016866593.1:p.Gln1257=
|
|
XM_017011105.2:c.3739C=
|
XP_016866594.1:p.Gln1247=
|
|
XM_017011106.2:c.3610C=
|
XP_016866595.1:p.Gln1204=
|
|
XM_017011107.2:c.3589C=
|
XP_016866596.1:p.Gln1197=
|
|
XR_002956289.1:n.3981C=
|
|
|
NM_001363725.2:c.1438C=
|
NP_001350654.1:p.Gln480=
|
|
NM_001371656.1:c.3817C=
|
NP_001358585.1:p.Gln1273=
|
|
NM_001374820.1:c.3817C=
|
NP_001361749.1:p.Gln1273=
|
|
NM_001374828.1:c.3937C=
MANE Select
|
NP_001361757.1:p.Gln1313=
|
|
NM_017519.3:c.3778C=
|
NP_059989.3:p.Gln1260=
|
|