ENST00000539261.6:c.56G>A
(MGP)
MANE Select
|
ENSP00000445907.1:p.Cys19Tyr
|
|
ENST00000648334.1:n.126-18271C>T
(C12orf60)
|
|
|
ENST00000228938.5:c.56G>A
(MGP)
|
ENSP00000228938.5:p.Cys19Tyr
|
|
ENST00000507170.2:n.119G>A
(MGP)
|
|
|
ENST00000527783.1:n.76-13433C>T
(C12orf60)
|
|
|
ENST00000533472.1:n.87-18271C>T
(C12orf60)
|
|
|
ENST00000539261.5:c.56G>A
(MGP)
|
ENSP00000445907.1:p.Cys19Tyr
|
|
ENST00000543822.1:n.21C>T
(C12orf60)
|
|
|
NM_000900.3:c.56G>A
(MGP)
|
NP_000891.2:p.Cys19Tyr
|
|
NM_001190839.1:c.56G>A
(MGP)
|
NP_001177768.1:p.Cys19Tyr
|
|
NM_000900.4:c.56G>A
(MGP)
|
NP_000891.2:p.Cys19Tyr
|
|
NM_001190839.2:c.56G>A
(MGP)
|
NP_001177768.1:p.Cys19Tyr
|
|
NM_000900.5:c.56G>A
(MGP)
MANE Select
|
NP_000891.2:p.Cys19Tyr
|
|
NM_001190839.3:c.56G>A
(MGP)
|
NP_001177768.1:p.Cys19Tyr
|
|