ENST00000331373.10:c.921T>C
MANE Select
|
ENSP00000331258.5:p.Phe307=
|
|
ENST00000614426.2:c.*717T>C
|
ENSP00000478821.2:n.*717T>C
|
|
ENST00000674646.1:c.639T>C
|
ENSP00000501703.1:p.Phe213=
|
|
ENST00000674676.1:c.639T>C
|
ENSP00000502544.1:p.Phe213=
|
|
ENST00000674782.1:c.*841T>C
|
ENSP00000501683.1:n.*841T>C
|
|
ENST00000674937.1:c.879T>C
|
ENSP00000501823.1:p.Phe293=
|
|
ENST00000675322.1:c.639T>C
|
ENSP00000502235.1:p.Phe213=
|
|
ENST00000675675.1:c.639T>C
|
ENSP00000501793.1:p.Phe213=
|
|
ENST00000676178.1:c.*706T>C
|
ENSP00000502007.1:n.*706T>C
|
|
ENST00000676193.1:c.921T>C
|
ENSP00000502774.1:p.Phe307=
|
|
ENST00000331373.9:c.921T>C
|
ENSP00000331258.5:p.Phe307=
|
|
ENST00000614426.1:c.921T>C
|
ENSP00000478821.1:p.Phe307=
|
|
NM_001277971.1:c.921T>C
|
NP_001264900.1:p.Phe307=
|
|
NM_032237.4:c.921T>C
|
NP_115613.1:p.Phe307=
|
|
XM_011544668.1:c.921T>C
|
XP_011542970.1:p.Phe307=
|
|
XM_011544669.1:c.921T>C
|
XP_011542971.1:p.Phe307=
|
|
NM_032237.5:c.921T>C
MANE Select
|
NP_115613.1:p.Phe307=
|
|
NM_001277971.2:c.921T>C
|
NP_001264900.1:p.Phe307=
|
|