ENST00000537228.6:c.428-18G=
|
ENSP00000445691.1:n.428-18G=
|
|
ENST00000543081.6:c.427+305G=
|
ENSP00000439103.2:n.427+305G=
|
|
ENST00000544516.6:c.157-573G=
|
ENSP00000439538.2:n.157-573G=
|
|
ENST00000545576.2:n.841G=
|
|
|
ENST00000696246.1:c.413-18G=
|
ENSP00000512504.1:n.413-18G=
|
|
ENST00000696271.1:n.852G=
|
|
|
ENST00000696272.1:c.425G=
|
ENSP00000512515.1:p.Cys142=
|
|
ENST00000696273.1:c.473G=
|
ENSP00000512516.1:p.Cys158=
|
|
ENST00000229335.11:c.440G=
MANE Select
|
ENSP00000229335.6:p.Cys147=
|
|
ENST00000229335.10:c.440G=
|
ENSP00000229335.6:p.Cys147=
|
|
ENST00000537228.5:c.428-18G=
|
ENSP00000445691.1:n.428-18G=
|
|
ENST00000543081.5:c.423+305G=
|
|
|
ENST00000544516.5:c.153-573G=
|
|
|
ENST00000545512.1:c.436G=
|
|
|
ENST00000545576.1:n.766G=
|
|
|
NM_020661.2:c.440G= , LRG_17t1:c.440G=
|
NP_065712.1:p.Cys147=
|
|
XM_011520772.1:c.428-18G=
|
XP_011519074.1:n.428-18G=
|
|
XM_011520773.1:c.427+305G=
|
XP_011519075.1:n.427+305G=
|
|
NM_001330343.1:c.428-18G=
|
NP_001317272.1:n.428-18G=
|
|
NM_020661.3:c.440G=
|
NP_065712.1:p.Cys147=
|
|
XM_011520773.2:c.427+305G=
|
XP_011519075.1:n.427+305G=
|
|
NM_020661.4:c.440G=
MANE Select
|
NP_065712.1:p.Cys147=
|
|
NM_001330343.2:c.428-18G=
|
NP_001317272.1:n.428-18G=
|
|