ENST00000265104.5:c.10620T>A
MANE Select
|
ENSP00000265104.4:p.Asp3540Glu
|
|
ENST00000681290.1:c.10575T>A
|
ENSP00000505288.1:p.Asp3525Glu
|
|
ENST00000265104.4:c.10620T>A
|
ENSP00000265104.4:p.Asp3540Glu
|
|
NM_001369.2:c.10620T>A
|
NP_001360.1:p.Asp3540Glu
|
|
XM_005248262.2:c.10575T>A
|
XP_005248319.1:p.Asp3525Glu
|
|
XM_005248262.3:c.10728T>A
|
XP_005248319.2:p.Asp3576Glu
|
|
XM_017009177.1:c.10728T>A
|
XP_016864666.1:p.Asp3576Glu
|
|
XM_017009178.1:c.9633T>A
|
XP_016864667.1:p.Asp3211Glu
|
|
XM_017009179.2:c.9633T>A
|
XP_016864668.1:p.Asp3211Glu
|
|
XM_017009180.1:c.10728T>A
|
XP_016864669.1:p.Asp3576Glu
|
|
XM_017009181.1:c.10728T>A
|
XP_016864670.1:p.Asp3576Glu
|
|
XM_017009182.1:c.10728T>A
|
XP_016864671.1:p.Asp3576Glu
|
|
XM_017009185.1:c.5817T>A
|
XP_016864674.1:p.Asp1939Glu
|
|
XM_017009186.1:c.5370T>A
|
XP_016864675.1:p.Asp1790Glu
|
|
XM_017009188.1:c.4707T>A
|
XP_016864677.1:p.Asp1569Glu
|
|
XM_024454388.1:c.9633T>A
|
XP_024310156.1:p.Asp3211Glu
|
|
XM_024454389.1:c.9222T>A
|
XP_024310157.1:p.Asp3074Glu
|
|
NM_001369.3:c.10620T>A
MANE Select
|
NP_001360.1:p.Asp3540Glu
|
|