ENST00000367049.9:c.770C>T
MANE Select
|
ENSP00000356016.4:p.Ser257Phe
|
|
ENST00000367051.6:c.487+12239C>T
|
ENSP00000356018.1:n.487+12239C>T
|
|
ENST00000367052.6:c.770C>T
|
ENSP00000356019.1:p.Ser257Phe
|
|
ENST00000367053.6:c.770C>T
|
ENSP00000356020.1:p.Ser257Phe
|
|
ENST00000400960.7:c.770C>T
|
ENSP00000383744.2:p.Ser257Phe
|
|
ENST00000367049.8:c.770C>T
|
ENSP00000356016.4:p.Ser257Phe
|
|
ENST00000367050.8:n.891C>T
|
|
|
ENST00000367051.5:c.487+12239C>T
|
ENSP00000356018.1:n.487+12239C>T
|
|
ENST00000367052.5:c.770C>T
|
ENSP00000356019.1:p.Ser257Phe
|
|
ENST00000367053.5:c.770C>T
|
ENSP00000356020.1:p.Ser257Phe
|
|
ENST00000400960.6:c.770C>T
|
ENSP00000383744.2:p.Ser257Phe
|
|
ENST00000434033.5:n.697C>T
|
|
|
ENST00000436595.1:n.414+12239C>T
|
|
|
ENST00000450439.5:n.697C>T
|
|
|
ENST00000529814.1:c.697C>T
|
|
|
ENST00000534202.5:c.770C>T
|
ENSP00000436139.2:p.Ser257Phe
|
|
NM_000573.3:c.770C>T
|
NP_000564.2:p.Ser257Phe
|
|
NM_000651.4:c.770C>T
|
NP_000642.3:p.Ser257Phe
|
|
XM_006711166.2:c.785C>T
|
XP_006711229.1:p.Ser262Phe
|
|
XM_011509205.1:c.785C>T
|
XP_011507507.1:p.Ser262Phe
|
|
NM_000651.5:c.770C>T
|
NP_000642.3:p.Ser257Phe
|
|
XM_024453287.1:c.785C>T
|
XP_024309055.1:p.Ser262Phe
|
|
NM_000573.4:c.770C>T
|
NP_000564.2:p.Ser257Phe
|
|
NM_000651.6:c.770C>T
MANE Select
|
NP_000642.3:p.Ser257Phe
|
|