ENST00000643759.2:c.7012G=
MANE Select
|
ENSP00000495214.1:p.Asp2338=
|
|
ENST00000368147.8:c.7012G=
|
ENSP00000357129.4:p.Asp2338=
|
|
ENST00000481212.5:n.453G=
|
|
|
ENST00000498708.1:n.444G=
|
|
|
ENST00000614909.4:c.7012G=
|
ENSP00000482595.1:p.Asp2338=
|
|
NM_003126.2:c.7012G=
|
NP_003117.2:p.Asp2338=
|
|
XM_011509916.1:c.7012G=
|
XP_011508218.1:p.Asp2338=
|
|
XM_011509917.1:c.6994G=
|
XP_011508219.1:p.Asp2332=
|
|
NM_003126.3:c.7012G=
|
NP_003117.2:p.Asp2338=
|
|
XM_011509916.2:c.7012G=
|
XP_011508218.1:p.Asp2338=
|
|
XM_011509917.3:c.6994G=
|
XP_011508219.1:p.Asp2332=
|
|
NM_003126.4:c.7012G=
MANE Select
|
NP_003117.2:p.Asp2338=
|
|