ENST00000265104.5:c.12695A>T
MANE Select
|
ENSP00000265104.4:p.Asp4232Val
|
|
ENST00000681290.1:c.12650A>T
|
ENSP00000505288.1:p.Asp4217Val
|
|
ENST00000265104.4:c.12695A>T
|
ENSP00000265104.4:p.Asp4232Val
|
|
NM_001369.2:c.12695A>T
|
NP_001360.1:p.Asp4232Val
|
|
XM_005248262.2:c.12650A>T
|
XP_005248319.1:p.Asp4217Val
|
|
XM_005248262.3:c.12803A>T
|
XP_005248319.2:p.Asp4268Val
|
|
XM_017009177.1:c.12803A>T
|
XP_016864666.1:p.Asp4268Val
|
|
XM_017009178.1:c.11708A>T
|
XP_016864667.1:p.Asp3903Val
|
|
XM_017009179.2:c.11708A>T
|
XP_016864668.1:p.Asp3903Val
|
|
XM_017009180.1:c.12803A>T
|
XP_016864669.1:p.Asp4268Val
|
|
XM_017009185.1:c.7892A>T
|
XP_016864674.1:p.Asp2631Val
|
|
XM_017009186.1:c.7445A>T
|
XP_016864675.1:p.Asp2482Val
|
|
XM_017009188.1:c.6782A>T
|
XP_016864677.1:p.Asp2261Val
|
|
XM_024454388.1:c.11708A>T
|
XP_024310156.1:p.Asp3903Val
|
|
XM_024454389.1:c.11297A>T
|
XP_024310157.1:p.Asp3766Val
|
|
NM_001369.3:c.12695A>T
MANE Select
|
NP_001360.1:p.Asp4232Val
|
|