ENST00000643759.2:c.638G>T
MANE Select
|
ENSP00000495214.1:p.Arg213Ile
|
|
ENST00000368147.8:c.638G>T
|
ENSP00000357129.4:p.Arg213Ile
|
|
ENST00000467387.1:c.133-2089G>T
|
ENSP00000476485.1:n.133-2089G>T
|
|
ENST00000614909.4:c.638G>T
|
ENSP00000482595.1:p.Arg213Ile
|
|
NM_003126.2:c.638G>T
|
NP_003117.2:p.Arg213Ile
|
|
XM_011509916.1:c.638G>T
|
XP_011508218.1:p.Arg213Ile
|
|
XM_011509917.1:c.638G>T
|
XP_011508219.1:p.Arg213Ile
|
|
XM_011509918.1:c.638G>T
|
XP_011508220.1:p.Arg213Ile
|
|
XM_011509919.1:c.638G>T
|
XP_011508221.1:p.Arg213Ile
|
|
XR_921911.1:n.751G>T
|
|
|
XR_921912.1:n.756G>T
|
|
|
NM_003126.3:c.638G>T
|
NP_003117.2:p.Arg213Ile
|
|
XM_011509916.2:c.638G>T
|
XP_011508218.1:p.Arg213Ile
|
|
XM_011509917.3:c.638G>T
|
XP_011508219.1:p.Arg213Ile
|
|
XM_011509918.3:c.638G>T
|
XP_011508220.1:p.Arg213Ile
|
|
XM_011509919.3:c.638G>T
|
XP_011508221.1:p.Arg213Ile
|
|
XR_921911.3:n.764G>T
|
|
|
XR_921912.2:n.766G>T
|
|
|
NM_003126.4:c.638G>T
MANE Select
|
NP_003117.2:p.Arg213Ile
|
|