ENST00000265104.5:c.10901G>C
MANE Select
|
ENSP00000265104.4:p.Arg3634Thr
|
|
ENST00000681290.1:c.10856G>C
|
ENSP00000505288.1:p.Arg3619Thr
|
|
ENST00000265104.4:c.10901G>C
|
ENSP00000265104.4:p.Arg3634Thr
|
|
NM_001369.2:c.10901G>C
|
NP_001360.1:p.Arg3634Thr
|
|
XM_005248262.2:c.10856G>C
|
XP_005248319.1:p.Arg3619Thr
|
|
XM_005248262.3:c.11009G>C
|
XP_005248319.2:p.Arg3670Thr
|
|
XM_017009177.1:c.11009G>C
|
XP_016864666.1:p.Arg3670Thr
|
|
XM_017009178.1:c.9914G>C
|
XP_016864667.1:p.Arg3305Thr
|
|
XM_017009179.2:c.9914G>C
|
XP_016864668.1:p.Arg3305Thr
|
|
XM_017009180.1:c.11009G>C
|
XP_016864669.1:p.Arg3670Thr
|
|
XM_017009181.1:c.11009G>C
|
XP_016864670.1:p.Arg3670Thr
|
|
XM_017009182.1:c.11009G>C
|
XP_016864671.1:p.Arg3670Thr
|
|
XM_017009185.1:c.6098G>C
|
XP_016864674.1:p.Arg2033Thr
|
|
XM_017009186.1:c.5651G>C
|
XP_016864675.1:p.Arg1884Thr
|
|
XM_017009188.1:c.4988G>C
|
XP_016864677.1:p.Arg1663Thr
|
|
XM_024454388.1:c.9914G>C
|
XP_024310156.1:p.Arg3305Thr
|
|
XM_024454389.1:c.9503G>C
|
XP_024310157.1:p.Arg3168Thr
|
|
NM_001369.3:c.10901G>C
MANE Select
|
NP_001360.1:p.Arg3634Thr
|
|