ENST00000312465.12:c.669G>C
MANE Select
|
ENSP00000311697.7:p.Glu223Asp
|
|
ENST00000312465.11:c.669G>C
|
ENSP00000311697.7:p.Glu223Asp
|
|
ENST00000456523.3:c.*193G>C
|
ENSP00000398353.3:n.*193G>C
|
|
ENST00000503413.1:n.618G>C
|
|
|
ENST00000507780.1:c.342+11522G>C
|
ENSP00000423903.1:n.342+11522G>C
|
|
NM_001291812.1:c.240G>C
|
NP_001278741.1:p.Glu80Asp
|
|
NM_004464.3:c.669G>C
|
NP_004455.2:p.Glu223Asp
|
|
NM_033143.2:c.*193G>C
|
NP_149134.1:n.*193G>C
|
|
NM_001291812.2:c.240G>C
|
NP_001278741.1:p.Glu80Asp
|
|
NM_004464.4:c.669G>C
MANE Select
|
NP_004455.2:p.Glu223Asp
|
|