ENST00000470918.2:n.4558A>T
|
|
|
ENST00000695970.1:c.3356A>T
|
ENSP00000512297.1:p.Tyr1119Phe
|
|
ENST00000695971.1:c.3509A>T
|
ENSP00000512298.1:p.Tyr1170Phe
|
|
ENST00000695972.1:c.*607A>T
|
ENSP00000512299.1:n.*607A>T
|
|
ENST00000695973.1:c.*1894A>T
|
ENSP00000512300.1:n.*1894A>T
|
|
ENST00000695974.1:c.3353A>T
|
ENSP00000512301.1:p.Tyr1118Phe
|
|
ENST00000695975.1:c.*1657A>T
|
ENSP00000512302.1:n.*1657A>T
|
|
ENST00000695976.1:c.3341A>T
|
ENSP00000512303.1:p.Tyr1114Phe
|
|
ENST00000695981.1:c.3530A>T
|
ENSP00000512306.1:p.Tyr1177Phe
|
|
ENST00000695984.1:c.1538A>T
|
ENSP00000512309.1:p.Tyr513Phe
|
|
ENST00000695986.1:c.*3181A>T
|
ENSP00000512311.1:n.*3181A>T
|
|
ENST00000695990.1:n.564A>T
|
|
|
ENST00000696026.1:c.*1812A>T
|
ENSP00000512335.1:n.*1812A>T
|
|
ENST00000696027.1:c.3524A>T
|
ENSP00000512336.1:p.Tyr1175Phe
|
|
ENST00000696028.1:c.3458A>T
|
ENSP00000512337.1:p.Tyr1153Phe
|
|
ENST00000696029.1:c.3524A>T
|
ENSP00000512338.1:p.Tyr1175Phe
|
|
ENST00000696031.1:c.*3048A>T
|
ENSP00000512340.1:n.*3048A>T
|
|
ENST00000696032.1:c.3530A>T
|
ENSP00000512341.1:p.Tyr1177Phe
|
|
ENST00000696033.1:c.1160-32650A>T
|
ENSP00000512342.1:n.1160-32650A>T
|
|
ENST00000367429.9:c.3530A>T
MANE Select
|
ENSP00000356399.4:p.Tyr1177Phe
|
|
ENST00000367429.8:c.3530A>T
|
ENSP00000356399.4:p.Tyr1177Phe
|
|
ENST00000466229.5:n.6628A>T
|
|
|
NM_000186.3:c.3530A>T , LRG_47t1:c.3530A>T
|
NP_000177.2:p.Tyr1177Phe
|
|
XR_001737134.2:n.3716A>T
|
|
|
NM_000186.4:c.3530A>T
MANE Select
|
NP_000177.2:p.Tyr1177Phe
|
|