ENST00000299314.12:c.138A>G
MANE Select
|
ENSP00000299314.7:p.Arg46=
|
|
ENST00000647144.1:n.258A>G
|
|
|
ENST00000299314.11:c.138A>G
|
ENSP00000299314.7:p.Arg46=
|
|
ENST00000392919.4:c.138A>G
|
ENSP00000376651.4:p.Arg46=
|
|
ENST00000549165.1:c.138A>G
|
ENSP00000450413.1:p.Arg46=
|
|
ENST00000549940.5:c.138A>G
|
ENSP00000449150.1:p.Arg46=
|
|
NM_024312.4:c.138A>G
|
NP_077288.2:p.Arg46=
|
|
XM_006719593.2:c.138A>G
|
XP_006719656.1:p.Arg46=
|
|
XM_011538731.1:c.57A>G
|
XP_011537033.1:p.Arg19=
|
|
XM_006719593.3:c.138A>G
|
XP_006719656.1:p.Arg46=
|
|
XM_011538731.2:c.57A>G
|
XP_011537033.1:p.Arg19=
|
|
XM_017019961.1:c.-79A>G
|
XP_016875450.1:n.-79A>G
|
|
XM_017019962.2:c.-1213A>G
|
XP_016875451.1:n.-1213A>G
|
|
NM_024312.5:c.138A>G
MANE Select
|
NP_077288.2:p.Arg46=
|
|