ENST00000350026.11:c.3876G=
|
ENSP00000055163.8:p.Gln1292=
|
|
ENST00000414678.8:c.3945G=
|
ENSP00000412835.3:p.Gln1315=
|
|
ENST00000637015.2:c.4164G=
|
ENSP00000489729.2:p.Gln1388=
|
|
ENST00000346085.10:c.3915G=
|
ENSP00000344546.5:p.Gln1305=
|
|
ENST00000350026.10:c.3627G=
|
ENSP00000055163.7:p.Gln1209=
|
|
ENST00000414678.7:c.2193G=
|
ENSP00000412835.2:p.Gln731=
|
|
ENST00000635849.1:c.1356G=
|
ENSP00000490948.1:p.Gln452=
|
|
ENST00000635957.1:c.990G=
|
ENSP00000490385.1:p.Gln330=
|
|
ENST00000636930.2:c.4035G=
MANE Select
|
ENSP00000490491.2:p.Gln1345=
|
|
ENST00000636940.1:n.2032G=
|
|
|
ENST00000637015.1:c.1403G=
|
|
|
ENST00000637568.1:c.1317G=
|
|
|
ENST00000637741.1:n.701G=
|
|
|
ENST00000637810.1:c.1377G=
|
ENSP00000489636.1:p.Gln459=
|
|
ENST00000637904.1:c.1536G=
|
ENSP00000490550.1:p.Gln512=
|
|
ENST00000647938.1:c.3666G=
|
ENSP00000498155.1:p.Gln1222=
|
|
ENST00000346085.9:c.3666G=
|
ENSP00000344546.4:p.Gln1222=
|
|
ENST00000350026.9:c.3627G=
|
ENSP00000055163.7:p.Gln1209=
|
|
ENST00000414678.6:c.2193G=
|
ENSP00000412835.2:p.Gln731=
|
|
NM_017519.2:c.3627G=
|
NP_059989.2:p.Gln1209=
|
|
NM_020732.3:c.3666G=
|
NP_065783.3:p.Gln1222=
|
|
XM_005267069.3:c.3786G=
|
XP_005267126.2:p.Gln1262=
|
|
XM_011535984.1:c.2865G=
|
XP_011534286.1:p.Gln955=
|
|
XM_011535985.1:c.2685G=
|
XP_011534287.1:p.Gln895=
|
|
XM_011535986.1:c.2445G=
|
XP_011534288.1:p.Gln815=
|
|
XM_011535987.1:c.2064G=
|
XP_011534289.1:p.Gln688=
|
|
XM_011535988.1:c.927G=
|
XP_011534290.1:p.Gln309=
|
|
NM_001346813.1:c.3786G=
|
NP_001333742.1:p.Gln1262=
|
|
NM_001363725.1:c.1536G=
|
NP_001350654.1:p.Gln512=
|
|
XM_011535984.2:c.3996G=
|
XP_011534286.2:p.Gln1332=
|
|
XM_011535988.3:c.927G=
|
XP_011534290.1:p.Gln309=
|
|
XM_017011103.2:c.3897G=
|
XP_016866592.1:p.Gln1299=
|
|
XM_017011104.1:c.3867G=
|
XP_016866593.1:p.Gln1289=
|
|
XM_017011105.2:c.3837G=
|
XP_016866594.1:p.Gln1279=
|
|
XM_017011106.2:c.3708G=
|
XP_016866595.1:p.Gln1236=
|
|
XM_017011107.2:c.3687G=
|
XP_016866596.1:p.Gln1229=
|
|
XR_002956289.1:n.4079G=
|
|
|
NM_001363725.2:c.1536G=
|
NP_001350654.1:p.Gln512=
|
|
NM_001371656.1:c.3915G=
|
NP_001358585.1:p.Gln1305=
|
|
NM_001374820.1:c.3915G=
|
NP_001361749.1:p.Gln1305=
|
|
NM_001374828.1:c.4035G=
MANE Select
|
NP_001361757.1:p.Gln1345=
|
|
NM_017519.3:c.3876G=
|
NP_059989.3:p.Gln1292=
|
|