ENST00000456935.7:c.2886C>A
MANE Select
|
ENSP00000395473.2:p.Arg962=
|
|
ENST00000221363.8:c.2883C>A
|
ENSP00000221363.4:p.Arg961=
|
|
ENST00000456935.6:c.2886C>A
|
ENSP00000395473.2:p.Arg962=
|
|
ENST00000466794.5:n.3476C>A
|
|
|
ENST00000469423.1:n.315C>A
|
|
|
ENST00000493218.5:n.297C>A
|
|
|
ENST00000597692.1:c.445C>A
|
|
|
NM_000528.3:c.2886C>A
|
NP_000519.2:p.Arg962=
|
|
NM_001173498.1:c.2883C>A
|
NP_001166969.1:p.Arg961=
|
|
XM_005259913.1:c.2889C>A
|
XP_005259970.1:p.Arg963=
|
|
XM_011528017.1:c.1785C>A
|
XP_011526319.1:p.Arg595=
|
|
XM_005259913.2:c.2889C>A
|
XP_005259970.1:p.Arg963=
|
|
XM_024451518.1:c.1785C>A
|
XP_024307286.1:p.Arg595=
|
|
NM_000528.4:c.2886C>A
MANE Select
|
NP_000519.2:p.Arg962=
|
|
NM_001173498.2:c.2883C>A
|
NP_001166969.1:p.Arg961=
|
|