ENST00000389266.8:c.961T>G
MANE Select
|
ENSP00000373918.3:p.Phe321Val
|
|
ENST00000444666.6:c.961T>G
|
ENSP00000415447.2:p.Phe321Val
|
|
ENST00000470392.2:n.1051T>G
|
|
|
ENST00000478124.6:n.1024T>G
|
|
|
ENST00000485784.2:n.1040T>G
|
|
|
ENST00000674616.1:c.*675T>G
|
ENSP00000502408.1:n.*675T>G
|
|
ENST00000674643.1:c.961T>G
|
ENSP00000501636.1:p.Phe321Val
|
|
ENST00000674734.1:n.1457T>G
|
|
|
ENST00000674737.1:c.*299T>G
|
ENSP00000502464.1:n.*299T>G
|
|
ENST00000674807.1:c.961T>G
|
ENSP00000502814.1:p.Phe321Val
|
|
ENST00000674815.1:c.592T>G
|
ENSP00000502799.1:p.Phe198Val
|
|
ENST00000674851.1:c.592T>G
|
ENSP00000502451.1:p.Phe198Val
|
|
ENST00000674969.1:n.2834T>G
|
|
|
ENST00000675051.1:c.760T>G
|
ENSP00000502296.1:p.Phe254Val
|
|
ENST00000675529.1:c.*831T>G
|
ENSP00000501655.1:n.*831T>G
|
|
ENST00000675587.1:n.977T>G
|
|
|
ENST00000675651.1:c.961T>G
|
ENSP00000502513.1:p.Phe321Val
|
|
ENST00000675693.1:c.793T>G
|
ENSP00000502174.1:p.Phe265Val
|
|
ENST00000675810.1:c.859T>G
|
ENSP00000502743.1:p.Phe287Val
|
|
ENST00000675859.1:c.961T>G
|
ENSP00000502033.1:p.Phe321Val
|
|
ENST00000675863.1:n.969T>G
|
|
|
ENST00000675886.1:n.7001T>G
|
|
|
ENST00000676088.1:c.*903T>G
|
ENSP00000501884.1:n.*903T>G
|
|
ENST00000676140.1:c.961T>G
|
ENSP00000502571.1:p.Phe321Val
|
|
ENST00000676164.1:c.*412T>G
|
ENSP00000501986.1:n.*412T>G
|
|
ENST00000676210.1:c.*250T>G
|
ENSP00000502373.1:n.*250T>G
|
|
ENST00000676259.1:c.*393T>G
|
ENSP00000501980.1:n.*393T>G
|
|
ENST00000676403.1:c.961T>G
|
ENSP00000502681.1:p.Phe321Val
|
|
ENST00000389266.7:c.961T>G
|
ENSP00000373918.3:p.Phe321Val
|
|
ENST00000478124.5:n.999T>G
|
|
|
NM_001316772.1:c.799T>G
|
NP_001303701.1:p.Phe267Val
|
|
NM_002047.2:c.961T>G , LRG_243t1:c.961T>G
|
NP_002038.2:p.Phe321Val
|
|
NM_002047.3:c.961T>G
|
NP_002038.2:p.Phe321Val
|
|
XM_006715686.1:c.592T>G
|
XP_006715749.1:p.Phe198Val
|
|
XM_006715686.2:c.592T>G
|
XP_006715749.1:p.Phe198Val
|
|
NM_002047.4:c.961T>G
MANE Select
|
NP_002038.2:p.Phe321Val
|
|