ENST00000683611.1:n.1110A>T
|
|
|
ENST00000265104.5:c.13777A>T
MANE Select
|
ENSP00000265104.4:p.Thr4593Ser
|
|
ENST00000681290.1:c.13732A>T
|
ENSP00000505288.1:p.Thr4578Ser
|
|
ENST00000265104.4:c.13777A>T
|
ENSP00000265104.4:p.Thr4593Ser
|
|
NM_001369.2:c.13777A>T
|
NP_001360.1:p.Thr4593Ser
|
|
XM_005248262.2:c.13732A>T
|
XP_005248319.1:p.Thr4578Ser
|
|
XM_005248262.3:c.13885A>T
|
XP_005248319.2:p.Thr4629Ser
|
|
XM_017009177.1:c.13465A>T
|
XP_016864666.1:p.Thr4489Ser
|
|
XM_017009178.1:c.12790A>T
|
XP_016864667.1:p.Thr4264Ser
|
|
XM_017009179.2:c.12790A>T
|
XP_016864668.1:p.Thr4264Ser
|
|
XM_017009185.1:c.8974A>T
|
XP_016864674.1:p.Thr2992Ser
|
|
XM_017009186.1:c.8527A>T
|
XP_016864675.1:p.Thr2843Ser
|
|
XM_017009188.1:c.7864A>T
|
XP_016864677.1:p.Thr2622Ser
|
|
XM_024454388.1:c.12790A>T
|
XP_024310156.1:p.Thr4264Ser
|
|
XM_024454389.1:c.12379A>T
|
XP_024310157.1:p.Thr4127Ser
|
|
NM_001369.3:c.13777A>T
MANE Select
|
NP_001360.1:p.Thr4593Ser
|
|