ENST00000350026.11:c.3789G>C
|
ENSP00000055163.8:p.Gln1263His
|
|
ENST00000414678.8:c.3858G>C
|
ENSP00000412835.3:p.Gln1286His
|
|
ENST00000637015.2:c.4077G>C
|
ENSP00000489729.2:p.Gln1359His
|
|
ENST00000346085.10:c.3828G>C
|
ENSP00000344546.5:p.Gln1276His
|
|
ENST00000350026.10:c.3540G>C
|
ENSP00000055163.7:p.Gln1180His
|
|
ENST00000414678.7:c.2106G>C
|
ENSP00000412835.2:p.Gln702His
|
|
ENST00000635849.1:c.1269G>C
|
ENSP00000490948.1:p.Gln423His
|
|
ENST00000635957.1:c.903G>C
|
ENSP00000490385.1:p.Gln301His
|
|
ENST00000636930.2:c.3948G>C
MANE Select
|
ENSP00000490491.2:p.Gln1316His
|
|
ENST00000636940.1:n.1945G>C
|
|
|
ENST00000637015.1:c.1316G>C
|
|
|
ENST00000637568.1:c.1230G>C
|
|
|
ENST00000637741.1:n.614G>C
|
|
|
ENST00000637810.1:c.1290G>C
|
ENSP00000489636.1:p.Gln430His
|
|
ENST00000637904.1:c.1449G>C
|
ENSP00000490550.1:p.Gln483His
|
|
ENST00000647938.1:c.3579G>C
|
ENSP00000498155.1:p.Gln1193His
|
|
ENST00000346085.9:c.3579G>C
|
ENSP00000344546.4:p.Gln1193His
|
|
ENST00000350026.9:c.3540G>C
|
ENSP00000055163.7:p.Gln1180His
|
|
ENST00000414678.6:c.2106G>C
|
ENSP00000412835.2:p.Gln702His
|
|
NM_017519.2:c.3540G>C
|
NP_059989.2:p.Gln1180His
|
|
NM_020732.3:c.3579G>C
|
NP_065783.3:p.Gln1193His
|
|
XM_005267069.3:c.3699G>C
|
XP_005267126.2:p.Gln1233His
|
|
XM_011535984.1:c.2778G>C
|
XP_011534286.1:p.Gln926His
|
|
XM_011535985.1:c.2598G>C
|
XP_011534287.1:p.Gln866His
|
|
XM_011535986.1:c.2358G>C
|
XP_011534288.1:p.Gln786His
|
|
XM_011535987.1:c.1977G>C
|
XP_011534289.1:p.Gln659His
|
|
XM_011535988.1:c.840G>C
|
XP_011534290.1:p.Gln280His
|
|
NM_001346813.1:c.3699G>C
|
NP_001333742.1:p.Gln1233His
|
|
NM_001363725.1:c.1449G>C
|
NP_001350654.1:p.Gln483His
|
|
XM_011535984.2:c.3909G>C
|
XP_011534286.2:p.Gln1303His
|
|
XM_011535988.3:c.840G>C
|
XP_011534290.1:p.Gln280His
|
|
XM_017011103.2:c.3810G>C
|
XP_016866592.1:p.Gln1270His
|
|
XM_017011104.1:c.3780G>C
|
XP_016866593.1:p.Gln1260His
|
|
XM_017011105.2:c.3750G>C
|
XP_016866594.1:p.Gln1250His
|
|
XM_017011106.2:c.3621G>C
|
XP_016866595.1:p.Gln1207His
|
|
XM_017011107.2:c.3600G>C
|
XP_016866596.1:p.Gln1200His
|
|
XR_002956289.1:n.3992G>C
|
|
|
NM_001363725.2:c.1449G>C
|
NP_001350654.1:p.Gln483His
|
|
NM_001371656.1:c.3828G>C
|
NP_001358585.1:p.Gln1276His
|
|
NM_001374820.1:c.3828G>C
|
NP_001361749.1:p.Gln1276His
|
|
NM_001374828.1:c.3948G>C
MANE Select
|
NP_001361757.1:p.Gln1316His
|
|
NM_017519.3:c.3789G>C
|
NP_059989.3:p.Gln1263His
|
|