ENST00000330377.3:c.482A>G
MANE Select
|
ENSP00000329312.2:p.Glu161Gly
|
|
ENST00000249053.3:c.*111A>G
|
ENSP00000249053.3:n.*111A>G
|
|
ENST00000330377.2:c.482A>G
|
ENSP00000329312.2:p.Glu161Gly
|
|
ENST00000438703.1:c.485A>G
|
ENSP00000403391.1:p.Glu162Gly
|
|
NM_020070.3:c.482A>G
|
NP_064455.1:p.Glu161Gly
|
|
NM_152855.2:c.*111A>G
|
NP_690594.1:n.*111A>G
|
|
XM_011530169.1:c.485A>G
|
XP_011528471.1:p.Glu162Gly
|
|
XM_011530169.2:c.485A>G
|
XP_011528471.1:p.Glu162Gly
|
|
NM_020070.4:c.482A>G
MANE Select
|
NP_064455.1:p.Glu161Gly
|
|
NM_001369906.1:c.485A>G
|
NP_001356835.1:p.Glu162Gly
|
|
NM_152855.3:c.*111A>G
|
NP_690594.1:n.*111A>G
|
|