ENST00000683611.1:n.1107C>A
|
|
|
ENST00000265104.5:c.13774C>A
MANE Select
|
ENSP00000265104.4:p.Arg4592=
|
|
ENST00000681290.1:c.13729C>A
|
ENSP00000505288.1:p.Arg4577=
|
|
ENST00000265104.4:c.13774C>A
|
ENSP00000265104.4:p.Arg4592=
|
|
NM_001369.2:c.13774C>A
|
NP_001360.1:p.Arg4592=
|
|
XM_005248262.2:c.13729C>A
|
XP_005248319.1:p.Arg4577=
|
|
XM_005248262.3:c.13882C>A
|
XP_005248319.2:p.Arg4628=
|
|
XM_017009177.1:c.13462C>A
|
XP_016864666.1:p.Arg4488=
|
|
XM_017009178.1:c.12787C>A
|
XP_016864667.1:p.Arg4263=
|
|
XM_017009179.2:c.12787C>A
|
XP_016864668.1:p.Arg4263=
|
|
XM_017009185.1:c.8971C>A
|
XP_016864674.1:p.Arg2991=
|
|
XM_017009186.1:c.8524C>A
|
XP_016864675.1:p.Arg2842=
|
|
XM_017009188.1:c.7861C>A
|
XP_016864677.1:p.Arg2621=
|
|
XM_024454388.1:c.12787C>A
|
XP_024310156.1:p.Arg4263=
|
|
XM_024454389.1:c.12376C>A
|
XP_024310157.1:p.Arg4126=
|
|
NM_001369.3:c.13774C>A
MANE Select
|
NP_001360.1:p.Arg4592=
|
|