ENST00000545712.7:c.675A>G
MANE Select
|
ENSP00000445920.1:p.Arg225=
|
|
ENST00000537496.5:c.*240A>G
|
ENSP00000444793.1:n.*240A>G
|
|
ENST00000540016.5:c.519A>G
|
ENSP00000474582.1:p.Arg173=
|
|
ENST00000541763.6:c.900A>G
|
ENSP00000474981.1:n.900A>G
|
|
ENST00000544051.5:c.*556A>G
|
ENSP00000438079.1:n.*556A>G
|
|
ENST00000545712.6:c.675A>G
|
ENSP00000445920.1:p.Arg225=
|
|
NM_052845.3:c.675A>G
|
NP_443077.1:p.Arg225=
|
|
NR_038118.1:n.835A>G
|
|
|
XM_011538266.1:c.*22A>G
|
XP_011536568.1:n.*22A>G
|
|
XM_011538267.1:c.*22A>G
|
XP_011536569.1:n.*22A>G
|
|
XM_011538268.1:c.402A>G
|
XP_011536570.1:p.Arg134=
|
|
XM_011538269.1:c.399A>G
|
XP_011536571.1:p.Arg133=
|
|
XM_011538267.3:c.*22A>G
|
XP_011536569.1:n.*22A>G
|
|
XM_011538268.2:c.402A>G
|
XP_011536570.1:p.Arg134=
|
|
XM_011538269.2:c.399A>G
|
XP_011536571.1:p.Arg133=
|
|
NM_052845.4:c.675A>G
MANE Select
|
NP_443077.1:p.Arg225=
|
|
NR_038118.2:n.786A>G
|
|
|