ENST00000502613.3:c.1146C>G
MANE Select
|
ENSP00000424668.2:p.Ala382=
|
|
ENST00000335016.9:c.1146C>G
|
ENSP00000334836.5:p.Ala382=
|
|
ENST00000389010.7:c.*122C>G
|
ENSP00000373662.3:n.*122C>G
|
|
ENST00000502613.1:c.223C>G
|
|
|
ENST00000502871.5:c.1146C>G
|
ENSP00000421768.1:p.Ala382=
|
|
ENST00000505725.1:n.428C>G
|
|
|
ENST00000628286.1:c.*122C>G
|
ENSP00000487317.1:n.*122C>G
|
|
NM_017593.3:c.1146C>G
|
NP_060063.2:p.Ala382=
|
|
NM_198892.1:c.1146C>G
|
NP_942595.1:p.Ala382=
|
|
XM_005263117.1:c.1146C>G
|
XP_005263174.1:p.Ala382=
|
|
XM_011532101.1:c.906C>G
|
XP_011530403.1:p.Ala302=
|
|
XM_011532102.1:c.1146C>G
|
XP_011530404.1:p.Ala382=
|
|
XM_017008381.1:c.906C>G
|
XP_016863870.1:p.Ala302=
|
|
XM_017008382.1:c.258C>G
|
XP_016863871.1:p.Ala86=
|
|
NM_017593.4:c.1146C>G
|
NP_060063.2:p.Ala382=
|
|
NM_017593.5:c.1146C>G
|
NP_060063.2:p.Ala382=
|
|
NM_198892.2:c.1146C>G
MANE Select
|
NP_942595.1:p.Ala382=
|
|