ENST00000261647.10:c.117G>C
MANE Select
|
ENSP00000261647.5:p.Glu39Asp
|
|
ENST00000261647.9:c.117G>C
|
ENSP00000261647.5:p.Glu39Asp
|
|
ENST00000466729.5:c.182G>C
|
|
|
ENST00000470399.1:c.132G>C
|
ENSP00000465082.1:p.Glu44Asp
|
|
ENST00000475723.5:c.164G>C
|
|
|
ENST00000497842.6:n.142G>C
|
|
|
ENST00000583704.1:n.142G>C
|
|
|
NM_001271420.1:c.-342G>C
|
NP_001258349.1:n.-342G>C
|
|
NM_017775.3:c.117G>C
|
NP_060245.3:p.Glu39Asp
|
|
XM_011523950.1:c.117G>C
|
XP_011522252.1:p.Glu39Asp
|
|
XM_017024801.2:c.117G>C
|
XP_016880290.2:p.Glu39Asp
|
|
XM_017024802.2:c.117G>C
|
XP_016880291.2:p.Glu39Asp
|
|
XM_024450814.1:c.117G>C
|
XP_024306582.1:p.Glu39Asp
|
|
NM_017775.4:c.117G>C
MANE Select
|
NP_060245.3:p.Glu39Asp
|
|
NM_001271420.2:c.-342G>C
|
NP_001258349.1:n.-342G>C
|
|