ENST00000265104.5:c.10878G>T
MANE Select
|
ENSP00000265104.4:p.Thr3626=
|
|
ENST00000681290.1:c.10833G>T
|
ENSP00000505288.1:p.Thr3611=
|
|
ENST00000265104.4:c.10878G>T
|
ENSP00000265104.4:p.Thr3626=
|
|
NM_001369.2:c.10878G>T
|
NP_001360.1:p.Thr3626=
|
|
XM_005248262.2:c.10833G>T
|
XP_005248319.1:p.Thr3611=
|
|
XM_005248262.3:c.10986G>T
|
XP_005248319.2:p.Thr3662=
|
|
XM_017009177.1:c.10986G>T
|
XP_016864666.1:p.Thr3662=
|
|
XM_017009178.1:c.9891G>T
|
XP_016864667.1:p.Thr3297=
|
|
XM_017009179.2:c.9891G>T
|
XP_016864668.1:p.Thr3297=
|
|
XM_017009180.1:c.10986G>T
|
XP_016864669.1:p.Thr3662=
|
|
XM_017009181.1:c.10986G>T
|
XP_016864670.1:p.Thr3662=
|
|
XM_017009182.1:c.10986G>T
|
XP_016864671.1:p.Thr3662=
|
|
XM_017009185.1:c.6075G>T
|
XP_016864674.1:p.Thr2025=
|
|
XM_017009186.1:c.5628G>T
|
XP_016864675.1:p.Thr1876=
|
|
XM_017009188.1:c.4965G>T
|
XP_016864677.1:p.Thr1655=
|
|
XM_024454388.1:c.9891G>T
|
XP_024310156.1:p.Thr3297=
|
|
XM_024454389.1:c.9480G>T
|
XP_024310157.1:p.Thr3160=
|
|
NM_001369.3:c.10878G>T
MANE Select
|
NP_001360.1:p.Thr3626=
|
|