ENST00000470918.2:n.4300G>T
|
|
|
ENST00000695970.1:c.3098G>T
|
ENSP00000512297.1:p.Cys1033Phe
|
|
ENST00000695971.1:c.3251G>T
|
ENSP00000512298.1:p.Cys1084Phe
|
|
ENST00000695972.1:c.*349G>T
|
ENSP00000512299.1:n.*349G>T
|
|
ENST00000695973.1:c.*1636G>T
|
ENSP00000512300.1:n.*1636G>T
|
|
ENST00000695974.1:c.3095G>T
|
ENSP00000512301.1:p.Cys1032Phe
|
|
ENST00000695975.1:c.*1399G>T
|
ENSP00000512302.1:n.*1399G>T
|
|
ENST00000695976.1:c.3083G>T
|
ENSP00000512303.1:p.Cys1028Phe
|
|
ENST00000695981.1:c.3272G>T
|
ENSP00000512306.1:p.Cys1091Phe
|
|
ENST00000695984.1:c.1280G>T
|
ENSP00000512309.1:p.Cys427Phe
|
|
ENST00000695986.1:c.*2923G>T
|
ENSP00000512311.1:n.*2923G>T
|
|
ENST00000696026.1:c.*1554G>T
|
ENSP00000512335.1:n.*1554G>T
|
|
ENST00000696027.1:c.3266G>T
|
ENSP00000512336.1:p.Cys1089Phe
|
|
ENST00000696028.1:c.3200G>T
|
ENSP00000512337.1:p.Cys1067Phe
|
|
ENST00000696029.1:c.3266G>T
|
ENSP00000512338.1:p.Cys1089Phe
|
|
ENST00000696031.1:c.*2790G>T
|
ENSP00000512340.1:n.*2790G>T
|
|
ENST00000696032.1:c.3272G>T
|
ENSP00000512341.1:p.Cys1091Phe
|
|
ENST00000696033.1:c.1160-36207G>T
|
ENSP00000512342.1:n.1160-36207G>T
|
|
ENST00000367429.9:c.3272G>T
MANE Select
|
ENSP00000356399.4:p.Cys1091Phe
|
|
ENST00000367429.8:c.3272G>T
|
ENSP00000356399.4:p.Cys1091Phe
|
|
ENST00000466229.5:n.6370G>T
|
|
|
NM_000186.3:c.3272G>T , LRG_47t1:c.3272G>T
|
NP_000177.2:p.Cys1091Phe
|
|
XR_001737134.2:n.3458G>T
|
|
|
NM_000186.4:c.3272G>T
MANE Select
|
NP_000177.2:p.Cys1091Phe
|
|