ENST00000683611.1:n.1115C>A
|
|
|
ENST00000265104.5:c.13782C>A
MANE Select
|
ENSP00000265104.4:p.Asp4594Glu
|
|
ENST00000681290.1:c.13737C>A
|
ENSP00000505288.1:p.Asp4579Glu
|
|
ENST00000265104.4:c.13782C>A
|
ENSP00000265104.4:p.Asp4594Glu
|
|
NM_001369.2:c.13782C>A
|
NP_001360.1:p.Asp4594Glu
|
|
XM_005248262.2:c.13737C>A
|
XP_005248319.1:p.Asp4579Glu
|
|
XM_005248262.3:c.13890C>A
|
XP_005248319.2:p.Asp4630Glu
|
|
XM_017009177.1:c.13470C>A
|
XP_016864666.1:p.Asp4490Glu
|
|
XM_017009178.1:c.12795C>A
|
XP_016864667.1:p.Asp4265Glu
|
|
XM_017009179.2:c.12795C>A
|
XP_016864668.1:p.Asp4265Glu
|
|
XM_017009185.1:c.8979C>A
|
XP_016864674.1:p.Asp2993Glu
|
|
XM_017009186.1:c.8532C>A
|
XP_016864675.1:p.Asp2844Glu
|
|
XM_017009188.1:c.7869C>A
|
XP_016864677.1:p.Asp2623Glu
|
|
XM_024454388.1:c.12795C>A
|
XP_024310156.1:p.Asp4265Glu
|
|
XM_024454389.1:c.12384C>A
|
XP_024310157.1:p.Asp4128Glu
|
|
NM_001369.3:c.13782C>A
MANE Select
|
NP_001360.1:p.Asp4594Glu
|
|