ENST00000683611.1:n.1139T=
|
|
|
ENST00000265104.5:c.13806T=
MANE Select
|
ENSP00000265104.4:p.Asp4602=
|
|
ENST00000681290.1:c.13761T=
|
ENSP00000505288.1:p.Asp4587=
|
|
ENST00000265104.4:c.13806T=
|
ENSP00000265104.4:p.Asp4602=
|
|
NM_001369.2:c.13806T=
|
NP_001360.1:p.Asp4602=
|
|
XM_005248262.2:c.13761T=
|
XP_005248319.1:p.Asp4587=
|
|
XM_005248262.3:c.13914T=
|
XP_005248319.2:p.Asp4638=
|
|
XM_017009177.1:c.13494T=
|
XP_016864666.1:p.Asp4498=
|
|
XM_017009178.1:c.12819T=
|
XP_016864667.1:p.Asp4273=
|
|
XM_017009179.2:c.12819T=
|
XP_016864668.1:p.Asp4273=
|
|
XM_017009185.1:c.9003T=
|
XP_016864674.1:p.Asp3001=
|
|
XM_017009186.1:c.8556T=
|
XP_016864675.1:p.Asp2852=
|
|
XM_017009188.1:c.7893T=
|
XP_016864677.1:p.Asp2631=
|
|
XM_024454388.1:c.12819T=
|
XP_024310156.1:p.Asp4273=
|
|
XM_024454389.1:c.12408T=
|
XP_024310157.1:p.Asp4136=
|
|
NM_001369.3:c.13806T=
MANE Select
|
NP_001360.1:p.Asp4602=
|
|