ENST00000362072.8:c.947A>G
MANE Select
|
ENSP00000354859.3:p.His316Arg
|
|
ENST00000346454.7:c.860A>G
|
ENSP00000278597.5:p.His287Arg
|
|
ENST00000362072.7:c.947A>G
|
ENSP00000354859.3:p.His316Arg
|
|
ENST00000538967.5:c.953A>G
|
ENSP00000438215.1:p.His318Arg
|
|
ENST00000542968.5:c.947A>G
|
ENSP00000442172.1:p.His316Arg
|
|
ENST00000544518.5:c.944A>G
|
ENSP00000441068.1:p.His315Arg
|
|
NM_000795.3:c.947A>G
|
NP_000786.1:p.His316Arg
|
|
NM_016574.3:c.860A>G
|
NP_057658.2:p.His287Arg
|
|
XM_017017296.2:c.947A>G
|
XP_016872785.1:p.His316Arg
|
|
NM_000795.4:c.947A>G
MANE Select
|
NP_000786.1:p.His316Arg
|
|
NM_016574.4:c.860A>G
|
NP_057658.2:p.His287Arg
|
|