ENST00000683611.1:n.547G>C
|
|
|
ENST00000265104.5:c.13214G>C
MANE Select
|
ENSP00000265104.4:p.Ser4405Thr
|
|
ENST00000681290.1:c.13169G>C
|
ENSP00000505288.1:p.Ser4390Thr
|
|
ENST00000265104.4:c.13214G>C
|
ENSP00000265104.4:p.Ser4405Thr
|
|
NM_001369.2:c.13214G>C
|
NP_001360.1:p.Ser4405Thr
|
|
XM_005248262.2:c.13169G>C
|
XP_005248319.1:p.Ser4390Thr
|
|
XM_005248262.3:c.13322G>C
|
XP_005248319.2:p.Ser4441Thr
|
|
XM_017009177.1:c.12902G>C
|
XP_016864666.1:p.Ser4301Thr
|
|
XM_017009178.1:c.12227G>C
|
XP_016864667.1:p.Ser4076Thr
|
|
XM_017009179.2:c.12227G>C
|
XP_016864668.1:p.Ser4076Thr
|
|
XM_017009185.1:c.8411G>C
|
XP_016864674.1:p.Ser2804Thr
|
|
XM_017009186.1:c.7964G>C
|
XP_016864675.1:p.Ser2655Thr
|
|
XM_017009188.1:c.7301G>C
|
XP_016864677.1:p.Ser2434Thr
|
|
XM_024454388.1:c.12227G>C
|
XP_024310156.1:p.Ser4076Thr
|
|
XM_024454389.1:c.11816G>C
|
XP_024310157.1:p.Ser3939Thr
|
|
NM_001369.3:c.13214G>C
MANE Select
|
NP_001360.1:p.Ser4405Thr
|
|