ENST00000683611.1:n.1157C>T
|
|
|
ENST00000265104.5:c.13824C>T
MANE Select
|
ENSP00000265104.4:p.Thr4608=
|
|
ENST00000681290.1:c.13779C>T
|
ENSP00000505288.1:p.Thr4593=
|
|
ENST00000265104.4:c.13824C>T
|
ENSP00000265104.4:p.Thr4608=
|
|
NM_001369.2:c.13824C>T
|
NP_001360.1:p.Thr4608=
|
|
XM_005248262.2:c.13779C>T
|
XP_005248319.1:p.Thr4593=
|
|
XM_005248262.3:c.13932C>T
|
XP_005248319.2:p.Thr4644=
|
|
XM_017009177.1:c.13512C>T
|
XP_016864666.1:p.Thr4504=
|
|
XM_017009178.1:c.12837C>T
|
XP_016864667.1:p.Thr4279=
|
|
XM_017009179.2:c.12837C>T
|
XP_016864668.1:p.Thr4279=
|
|
XM_017009185.1:c.9021C>T
|
XP_016864674.1:p.Thr3007=
|
|
XM_017009186.1:c.8574C>T
|
XP_016864675.1:p.Thr2858=
|
|
XM_017009188.1:c.7911C>T
|
XP_016864677.1:p.Thr2637=
|
|
XM_024454388.1:c.12837C>T
|
XP_024310156.1:p.Thr4279=
|
|
XM_024454389.1:c.12426C>T
|
XP_024310157.1:p.Thr4142=
|
|
NM_001369.3:c.13824C>T
MANE Select
|
NP_001360.1:p.Thr4608=
|
|