ENST00000480775.3:c.571G>C
|
ENSP00000485462.2:p.Asp191His
|
|
ENST00000623287.4:c.446G>C
|
ENSP00000485437.1:p.Arg149Thr
|
|
ENST00000623632.4:c.571G>C
|
ENSP00000485288.2:p.Asp191His
|
|
ENST00000625194.4:c.571G>C
|
ENSP00000485289.2:p.Asp191His
|
|
ENST00000636124.1:n.263G>C
|
|
|
ENST00000636265.1:c.571G>C
|
ENSP00000490909.1:p.Asp191His
|
|
ENST00000636433.1:n.593G>C
|
|
|
ENST00000636714.1:c.571G>C
|
ENSP00000490946.1:p.Asp191His
|
|
ENST00000637666.2:c.571G>C
|
ENSP00000489696.2:p.Asp191His
|
|
ENST00000637669.1:c.571G>C
|
ENSP00000489728.1:p.Asp191His
|
|
ENST00000639722.1:c.*267G>C
|
ENSP00000492828.1:n.*267G>C
|
|
ENST00000674592.1:n.595G>C
|
|
|
ENST00000675622.1:n.3638G>C
|
|
|
ENST00000679609.1:c.446G>C
|
ENSP00000506592.1:p.Arg149Thr
|
|
ENST00000679656.1:n.476G>C
|
|
|
ENST00000679723.1:c.526G>C
|
ENSP00000505155.1:p.Asp176His
|
|
ENST00000679845.1:n.694G>C
|
|
|
ENST00000679904.1:n.558G>C
|
|
|
ENST00000680378.1:c.658G>C
|
ENSP00000505556.1:p.Asp220His
|
|
ENST00000680444.1:c.571G>C
|
ENSP00000505298.1:p.Asp191His
|
|
ENST00000680978.1:c.571G>C
|
ENSP00000505244.1:p.Asp191His
|
|
ENST00000681159.1:n.630G>C
|
|
|
ENST00000216194.11:c.613G>C
|
ENSP00000216194.8:p.Asp205His
|
|
ENST00000342312.9:c.571G>C
|
ENSP00000341429.6:p.Asp191His
|
|
ENST00000477111.2:n.476G>C
|
|
|
ENST00000623063.3:c.571G>C
MANE Select
|
ENSP00000485525.1:p.Asp191His
|
|
ENST00000623287.3:c.446G>C
|
ENSP00000485437.1:p.Arg149Thr
|
|
ENST00000623632.3:c.526G>C
|
ENSP00000485288.1:p.Asp176His
|
|
ENST00000623978.3:c.31G>C
|
ENSP00000485477.1:p.Asp11His
|
|
ENST00000624474.1:c.491G>C
|
ENSP00000485286.1:p.Arg164Thr
|
|
ENST00000625194.3:c.158G>C
|
|
|
NM_000026.2:c.571G>C
|
NP_000017.1:p.Asp191His
|
|
NM_001123378.1:c.571G>C
|
NP_001116850.1:p.Asp191His
|
|
XM_011529976.1:c.571G>C
|
XP_011528278.1:p.Asp191His
|
|
XM_011529977.1:c.571G>C
|
XP_011528279.1:p.Asp191His
|
|
XM_011529978.1:c.571G>C
|
XP_011528280.1:p.Asp191His
|
|
XM_011529979.1:c.571G>C
|
XP_011528281.1:p.Asp191His
|
|
XM_011529980.1:c.571G>C
|
XP_011528282.1:p.Asp191His
|
|
XM_011529981.1:c.106G>C
|
XP_011528283.1:p.Asp36His
|
|
XR_937824.1:n.630G>C
|
|
|
XR_937825.1:n.630G>C
|
|
|
XR_937826.1:n.630G>C
|
|
|
NM_000026.3:c.571G>C
|
NP_000017.1:p.Asp191His
|
|
NM_001123378.2:c.571G>C
|
NP_001116850.1:p.Asp191His
|
|
NM_001317923.1:c.379G>C
|
NP_001304852.1:p.Asp127His
|
|
NM_001363840.1:c.571G>C
|
NP_001350769.1:p.Asp191His
|
|
NR_134256.1:n.630G>C
|
|
|
XM_011529977.3:c.571G>C
|
XP_011528279.1:p.Asp191His
|
|
XM_011529980.3:c.571G>C
|
XP_011528282.1:p.Asp191His
|
|
XM_017028636.1:c.526G>C
|
XP_016884125.1:p.Asp176His
|
|
XM_017028637.1:c.526G>C
|
XP_016884126.1:p.Asp176His
|
|
XM_017028638.1:c.106G>C
|
XP_016884127.1:p.Asp36His
|
|
XM_017028639.2:c.106G>C
|
XP_016884128.1:p.Asp36His
|
|
XM_024452166.1:c.526G>C
|
XP_024307934.1:p.Asp176His
|
|
XR_001755176.2:n.628G>C
|
|
|
XR_002958670.1:n.567G>C
|
|
|
XR_002958671.1:n.628G>C
|
|
|
XR_937825.3:n.628G>C
|
|
|
NM_000026.4:c.571G>C
MANE Select
|
NP_000017.1:p.Asp191His
|
|
NM_001363840.2:c.571G>C
|
NP_001350769.1:p.Asp191His
|
|
NM_001123378.3:c.571G>C
|
NP_001116850.1:p.Asp191His
|
|
NM_001317923.2:c.379G>C
|
NP_001304852.1:p.Asp127His
|
|
NM_001363840.3:c.571G>C
|
NP_001350769.1:p.Asp191His
|
|
NR_134256.2:n.630G>C
|
|
|