ENST00000355832.10:c.486C>T
MANE Select
|
ENSP00000348089.5:p.Ala162=
|
|
ENST00000447839.7:c.486C>T
MANE Plus Clinical
|
ENSP00000387966.2:p.Ala162=
|
|
ENST00000679596.1:c.*172+1766C>T
|
ENSP00000504862.1:n.*172+1766C>T
|
|
ENST00000679811.1:n.569C>T
|
|
|
ENST00000680107.1:c.486C>T
|
ENSP00000505909.1:p.Ala162=
|
|
ENST00000680233.1:n.579C>T
|
|
|
ENST00000681632.1:n.564C>T
|
|
|
ENST00000681659.1:c.486C>T
|
ENSP00000505631.1:p.Ala162=
|
|
ENST00000355832.9:c.486C>T
|
ENSP00000348089.5:p.Ala162=
|
|
ENST00000447839.6:c.486C>T
|
ENSP00000387966.2:p.Ala162=
|
|
ENST00000462247.1:c.486C>T
|
ENSP00000422827.1:p.Ala162=
|
|
ENST00000515869.1:c.486C>T
|
ENSP00000423550.1:p.Ala162=
|
|
NM_000124.3:c.486C>T
|
NP_000115.1:p.Ala162=
|
|
NM_001277058.1:c.486C>T
|
NP_001263987.1:p.Ala162=
|
|
NM_001277059.1:c.486C>T
|
NP_001263988.1:p.Ala162=
|
|
NM_001346440.1:c.486C>T
|
NP_001333369.1:p.Ala162=
|
|
NM_000124.4:c.486C>T
MANE Select
|
NP_000115.1:p.Ala162=
|
|
NM_001277058.2:c.486C>T
MANE Plus Clinical
|
NP_001263987.1:p.Ala162=
|
|
NM_001277059.2:c.486C>T
|
NP_001263988.1:p.Ala162=
|
|
NM_001346440.2:c.486C>T
|
NP_001333369.1:p.Ala162=
|
|