ENST00000247138.11:c.1136A>T
MANE Select
|
ENSP00000247138.5:p.Asp379Val
|
|
ENST00000247138.10:c.1136A>T
|
ENSP00000247138.5:p.Asp379Val
|
|
ENST00000376515.8:c.474A>T
|
ENSP00000365698.3:p.Arg158Ser
|
|
ENST00000376521.6:c.1136A>T
|
ENSP00000365704.1:p.Asp379Val
|
|
ENST00000376529.8:c.546A>T
|
ENSP00000365712.3:p.Arg182Ser
|
|
ENST00000413561.7:c.698A>T
|
|
|
ENST00000445167.7:c.546A>T
|
ENSP00000402726.2:p.Arg182Ser
|
|
ENST00000452555.7:c.1220A>T
|
ENSP00000416002.2:p.Asp407Val
|
|
ENST00000616181.5:c.1175A>T
|
ENSP00000478617.1:p.Asp392Val
|
|
ENST00000635285.1:c.1136A>T
|
ENSP00000489484.1:p.Asp379Val
|
|
ENST00000635460.1:c.425-1308A>T
|
|
|
ENST00000635589.1:c.953A>T
|
ENSP00000489197.1:p.Asp318Val
|
|
ENST00000635628.1:c.*1030A>T
|
ENSP00000489613.1:n.*1030A>T
|
|
NM_001032289.2:c.546A>T
|
NP_001027460.1:p.Arg182Ser
|
|
NM_001042498.2:c.1136A>T
|
NP_001035963.1:p.Asp379Val
|
|
NM_001282647.1:c.546A>T
|
NP_001269576.1:p.Arg182Ser
|
|
NM_001282648.1:c.474A>T
|
NP_001269577.1:p.Arg158Ser
|
|
NM_001282649.1:c.953A>T
|
NP_001269578.1:p.Asp318Val
|
|
NM_001282650.1:c.1175A>T
|
NP_001269579.1:p.Asp392Val
|
|
NM_001282651.1:c.1220A>T
|
NP_001269580.1:p.Asp407Val
|
|
NM_005660.2:c.1136A>T
|
NP_005651.1:p.Asp379Val
|
|
NM_005660.3:c.1136A>T
MANE Select
|
NP_005651.1:p.Asp379Val
|
|
NM_001032289.3:c.546A>T
|
NP_001027460.1:p.Arg182Ser
|
|
NM_001042498.3:c.1136A>T
|
NP_001035963.1:p.Asp379Val
|
|
NM_001282647.2:c.546A>T
|
NP_001269576.1:p.Arg182Ser
|
|
NM_001282649.2:c.953A>T
|
NP_001269578.1:p.Asp318Val
|
|
NM_001282650.2:c.1175A>T
|
NP_001269579.1:p.Asp392Val
|
|
NM_001282651.2:c.1220A>T
|
NP_001269580.1:p.Asp407Val
|
|
NM_001282648.2:c.474A>T
|
NP_001269577.1:p.Arg158Ser
|
|