ENST00000456935.7:c.2369A>G
MANE Select
|
ENSP00000395473.2:p.Gln790Arg
|
|
ENST00000221363.8:c.2366A>G
|
ENSP00000221363.4:p.Gln789Arg
|
|
ENST00000456935.6:c.2369A>G
|
ENSP00000395473.2:p.Gln790Arg
|
|
ENST00000466794.5:n.2959A>G
|
|
|
NM_000528.3:c.2369A>G
|
NP_000519.2:p.Gln790Arg
|
|
NM_001173498.1:c.2366A>G
|
NP_001166969.1:p.Gln789Arg
|
|
XM_005259913.1:c.2372A>G
|
XP_005259970.1:p.Gln791Arg
|
|
XM_011528017.1:c.1268A>G
|
XP_011526319.1:p.Gln423Arg
|
|
XM_005259913.2:c.2372A>G
|
XP_005259970.1:p.Gln791Arg
|
|
XM_024451518.1:c.1268A>G
|
XP_024307286.1:p.Gln423Arg
|
|
NM_000528.4:c.2369A>G
MANE Select
|
NP_000519.2:p.Gln790Arg
|
|
NM_001173498.2:c.2366A>G
|
NP_001166969.1:p.Gln789Arg
|
|