ENST00000265104.5:c.12597C>A
MANE Select
|
ENSP00000265104.4:p.Arg4199=
|
|
ENST00000681290.1:c.12552C>A
|
ENSP00000505288.1:p.Arg4184=
|
|
ENST00000265104.4:c.12597C>A
|
ENSP00000265104.4:p.Arg4199=
|
|
NM_001369.2:c.12597C>A
|
NP_001360.1:p.Arg4199=
|
|
XM_005248262.2:c.12552C>A
|
XP_005248319.1:p.Arg4184=
|
|
XM_005248262.3:c.12705C>A
|
XP_005248319.2:p.Arg4235=
|
|
XM_017009177.1:c.12705C>A
|
XP_016864666.1:p.Arg4235=
|
|
XM_017009178.1:c.11610C>A
|
XP_016864667.1:p.Arg3870=
|
|
XM_017009179.2:c.11610C>A
|
XP_016864668.1:p.Arg3870=
|
|
XM_017009180.1:c.12705C>A
|
XP_016864669.1:p.Arg4235=
|
|
XM_017009185.1:c.7794C>A
|
XP_016864674.1:p.Arg2598=
|
|
XM_017009186.1:c.7347C>A
|
XP_016864675.1:p.Arg2449=
|
|
XM_017009188.1:c.6684C>A
|
XP_016864677.1:p.Arg2228=
|
|
XM_024454388.1:c.11610C>A
|
XP_024310156.1:p.Arg3870=
|
|
XM_024454389.1:c.11199C>A
|
XP_024310157.1:p.Arg3733=
|
|
NM_001369.3:c.12597C>A
MANE Select
|
NP_001360.1:p.Arg4199=
|
|