ENST00000362072.8:c.934C>A
MANE Select
|
ENSP00000354859.3:p.His312Asn
|
|
ENST00000346454.7:c.847C>A
|
ENSP00000278597.5:p.His283Asn
|
|
ENST00000362072.7:c.934C>A
|
ENSP00000354859.3:p.His312Asn
|
|
ENST00000538967.5:c.940C>A
|
ENSP00000438215.1:p.His314Asn
|
|
ENST00000542968.5:c.934C>A
|
ENSP00000442172.1:p.His312Asn
|
|
ENST00000544518.5:c.931C>A
|
ENSP00000441068.1:p.His311Asn
|
|
NM_000795.3:c.934C>A
|
NP_000786.1:p.His312Asn
|
|
NM_016574.3:c.847C>A
|
NP_057658.2:p.His283Asn
|
|
XM_017017296.2:c.934C>A
|
XP_016872785.1:p.His312Asn
|
|
NM_000795.4:c.934C>A
MANE Select
|
NP_000786.1:p.His312Asn
|
|
NM_016574.4:c.847C>A
|
NP_057658.2:p.His283Asn
|
|