ENST00000545399.6:c.918T>C
|
ENSP00000444688.1:p.Gly306=
|
|
ENST00000644613.1:c.879T>C
|
ENSP00000494711.1:p.Gly293=
|
|
ENST00000648268.1:c.879T>C
MANE Select
|
ENSP00000498113.1:p.Gly293=
|
|
ENST00000302102.9:c.879T>C
|
ENSP00000302397.5:p.Gly293=
|
|
ENST00000441343.5:c.879T>C
|
ENSP00000411503.1:p.Gly293=
|
|
ENST00000485672.2:n.192T>C
|
|
|
ENST00000543770.5:c.912T>C
|
ENSP00000437577.1:p.Gly304=
|
|
ENST00000545399.5:c.918T>C
|
ENSP00000444688.1:p.Gly306=
|
|
ENST00000602133.5:c.789T>C
|
ENSP00000471581.1:p.Gly263=
|
|
NM_001256213.1:c.912T>C
|
NP_001243142.1:p.Gly304=
|
|
NM_001256214.1:c.918T>C
|
NP_001243143.1:p.Gly306=
|
|
NM_152296.4:c.879T>C
|
NP_689509.1:p.Gly293=
|
|
XM_011526991.1:c.789T>C
|
XP_011525293.1:p.Gly263=
|
|
NM_152296.5:c.879T>C
MANE Select
|
NP_689509.1:p.Gly293=
|
|
NM_001256214.2:c.918T>C
|
NP_001243143.1:p.Gly306=
|
|
NM_001256213.2:c.912T>C
|
NP_001243142.1:p.Gly304=
|
|