ENST00000683611.1:n.1126T>C
|
|
|
ENST00000265104.5:c.13793T>C
MANE Select
|
ENSP00000265104.4:p.Ile4598Thr
|
|
ENST00000681290.1:c.13748T>C
|
ENSP00000505288.1:p.Ile4583Thr
|
|
ENST00000265104.4:c.13793T>C
|
ENSP00000265104.4:p.Ile4598Thr
|
|
NM_001369.2:c.13793T>C
|
NP_001360.1:p.Ile4598Thr
|
|
XM_005248262.2:c.13748T>C
|
XP_005248319.1:p.Ile4583Thr
|
|
XM_005248262.3:c.13901T>C
|
XP_005248319.2:p.Ile4634Thr
|
|
XM_017009177.1:c.13481T>C
|
XP_016864666.1:p.Ile4494Thr
|
|
XM_017009178.1:c.12806T>C
|
XP_016864667.1:p.Ile4269Thr
|
|
XM_017009179.2:c.12806T>C
|
XP_016864668.1:p.Ile4269Thr
|
|
XM_017009185.1:c.8990T>C
|
XP_016864674.1:p.Ile2997Thr
|
|
XM_017009186.1:c.8543T>C
|
XP_016864675.1:p.Ile2848Thr
|
|
XM_017009188.1:c.7880T>C
|
XP_016864677.1:p.Ile2627Thr
|
|
XM_024454388.1:c.12806T>C
|
XP_024310156.1:p.Ile4269Thr
|
|
XM_024454389.1:c.12395T>C
|
XP_024310157.1:p.Ile4132Thr
|
|
NM_001369.3:c.13793T>C
MANE Select
|
NP_001360.1:p.Ile4598Thr
|
|