ENST00000265104.5:c.9794G>C
MANE Select
|
ENSP00000265104.4:p.Arg3265Thr
|
|
ENST00000681290.1:c.9749G>C
|
ENSP00000505288.1:p.Arg3250Thr
|
|
ENST00000265104.4:c.9794G>C
|
ENSP00000265104.4:p.Arg3265Thr
|
|
ENST00000504001.3:n.506G>C
|
|
|
NM_001369.2:c.9794G>C
|
NP_001360.1:p.Arg3265Thr
|
|
XM_005248262.2:c.9749G>C
|
XP_005248319.1:p.Arg3250Thr
|
|
XM_005248262.3:c.9902G>C
|
XP_005248319.2:p.Arg3301Thr
|
|
XM_017009177.1:c.9902G>C
|
XP_016864666.1:p.Arg3301Thr
|
|
XM_017009178.1:c.8807G>C
|
XP_016864667.1:p.Arg2936Thr
|
|
XM_017009179.2:c.8807G>C
|
XP_016864668.1:p.Arg2936Thr
|
|
XM_017009180.1:c.9902G>C
|
XP_016864669.1:p.Arg3301Thr
|
|
XM_017009181.1:c.9902G>C
|
XP_016864670.1:p.Arg3301Thr
|
|
XM_017009182.1:c.9902G>C
|
XP_016864671.1:p.Arg3301Thr
|
|
XM_017009185.1:c.4991G>C
|
XP_016864674.1:p.Arg1664Thr
|
|
XM_017009186.1:c.4544G>C
|
XP_016864675.1:p.Arg1515Thr
|
|
XM_017009188.1:c.3881G>C
|
XP_016864677.1:p.Arg1294Thr
|
|
XM_024454388.1:c.8807G>C
|
XP_024310156.1:p.Arg2936Thr
|
|
XM_024454389.1:c.8396G>C
|
XP_024310157.1:p.Arg2799Thr
|
|
NM_001369.3:c.9794G>C
MANE Select
|
NP_001360.1:p.Arg3265Thr
|
|