ENST00000561568.6:c.584A>G
|
ENSP00000457322.2:p.His195Arg
|
|
ENST00000565662.6:c.*102A>G
|
ENSP00000513729.1:n.*102A>G
|
|
ENST00000698444.1:c.470A>G
|
ENSP00000513726.1:p.His157Arg
|
|
ENST00000698445.1:c.517A>G
|
ENSP00000513727.1:p.Thr173Ala
|
|
ENST00000698446.1:c.*314A>G
|
ENSP00000513728.1:n.*314A>G
|
|
ENST00000698447.1:c.*280A>G
|
ENSP00000513732.1:n.*280A>G
|
|
ENST00000219281.8:c.623A>G
MANE Select
|
ENSP00000219281.3:p.His208Arg
|
|
ENST00000219281.7:c.623A>G
|
ENSP00000219281.3:p.His208Arg
|
|
ENST00000539737.6:c.569A>G
|
ENSP00000446143.2:p.His190Arg
|
|
ENST00000561743.5:c.470A>G
|
ENSP00000454928.1:p.His157Arg
|
|
ENST00000565151.1:n.818A>G
|
|
|
ENST00000565662.5:n.668A>G
|
|
|
ENST00000566082.1:n.2341A>G
|
|
|
NM_001195302.1:c.569A>G
|
NP_001182231.1:p.His190Arg
|
|
NM_024598.3:c.623A>G , LRG_352t1:c.623A>G
|
NP_078874.2:p.His208Arg
|
|
XM_005256144.3:c.470A>G
|
XP_005256201.1:p.His157Arg
|
|
XM_011523328.1:c.584A>G
|
XP_011521630.1:p.His195Arg
|
|
XM_011523329.1:c.470A>G
|
XP_011521631.1:p.His157Arg
|
|
NM_001330568.1:c.470A>G
|
NP_001317497.1:p.His157Arg
|
|
NM_001195302.2:c.569A>G
|
NP_001182231.1:p.His190Arg
|
|
NM_001330568.2:c.470A>G
|
NP_001317497.1:p.His157Arg
|
|
NM_024598.4:c.623A>G
MANE Select
|
NP_078874.2:p.His208Arg
|
|