ENST00000312465.12:c.629A>G
MANE Select
|
ENSP00000311697.7:p.His210Arg
|
|
ENST00000312465.11:c.629A>G
|
ENSP00000311697.7:p.His210Arg
|
|
ENST00000456523.3:c.*153A>G
|
ENSP00000398353.3:n.*153A>G
|
|
ENST00000503413.1:n.578A>G
|
|
|
ENST00000507780.1:c.342+11482A>G
|
ENSP00000423903.1:n.342+11482A>G
|
|
NM_001291812.1:c.200A>G
|
NP_001278741.1:p.His67Arg
|
|
NM_004464.3:c.629A>G
|
NP_004455.2:p.His210Arg
|
|
NM_033143.2:c.*153A>G
|
NP_149134.1:n.*153A>G
|
|
NM_001291812.2:c.200A>G
|
NP_001278741.1:p.His67Arg
|
|
NM_004464.4:c.629A>G
MANE Select
|
NP_004455.2:p.His210Arg
|
|