ENST00000683611.1:n.539G>T
|
|
|
ENST00000265104.5:c.13206G>T
MANE Select
|
ENSP00000265104.4:p.Arg4402Ser
|
|
ENST00000681290.1:c.13161G>T
|
ENSP00000505288.1:p.Arg4387Ser
|
|
ENST00000265104.4:c.13206G>T
|
ENSP00000265104.4:p.Arg4402Ser
|
|
NM_001369.2:c.13206G>T
|
NP_001360.1:p.Arg4402Ser
|
|
XM_005248262.2:c.13161G>T
|
XP_005248319.1:p.Arg4387Ser
|
|
XM_005248262.3:c.13314G>T
|
XP_005248319.2:p.Arg4438Ser
|
|
XM_017009177.1:c.12894G>T
|
XP_016864666.1:p.Arg4298Ser
|
|
XM_017009178.1:c.12219G>T
|
XP_016864667.1:p.Arg4073Ser
|
|
XM_017009179.2:c.12219G>T
|
XP_016864668.1:p.Arg4073Ser
|
|
XM_017009185.1:c.8403G>T
|
XP_016864674.1:p.Arg2801Ser
|
|
XM_017009186.1:c.7956G>T
|
XP_016864675.1:p.Arg2652Ser
|
|
XM_017009188.1:c.7293G>T
|
XP_016864677.1:p.Arg2431Ser
|
|
XM_024454388.1:c.12219G>T
|
XP_024310156.1:p.Arg4073Ser
|
|
XM_024454389.1:c.11808G>T
|
XP_024310157.1:p.Arg3936Ser
|
|
NM_001369.3:c.13206G>T
MANE Select
|
NP_001360.1:p.Arg4402Ser
|
|