ENST00000502613.3:c.1165A>G
MANE Select
|
ENSP00000424668.2:p.Ile389Val
|
|
ENST00000335016.9:c.1165A>G
|
ENSP00000334836.5:p.Ile389Val
|
|
ENST00000389010.7:c.*141A>G
|
ENSP00000373662.3:n.*141A>G
|
|
ENST00000502613.1:c.242A>G
|
|
|
ENST00000502871.5:c.1165A>G
|
ENSP00000421768.1:p.Ile389Val
|
|
ENST00000505725.1:n.447A>G
|
|
|
ENST00000628286.1:c.*141A>G
|
ENSP00000487317.1:n.*141A>G
|
|
NM_017593.3:c.1165A>G
|
NP_060063.2:p.Ile389Val
|
|
NM_198892.1:c.1165A>G
|
NP_942595.1:p.Ile389Val
|
|
XM_005263117.1:c.1165A>G
|
XP_005263174.1:p.Ile389Val
|
|
XM_011532101.1:c.925A>G
|
XP_011530403.1:p.Ile309Val
|
|
XM_011532102.1:c.1165A>G
|
XP_011530404.1:p.Ile389Val
|
|
XM_017008381.1:c.925A>G
|
XP_016863870.1:p.Ile309Val
|
|
XM_017008382.1:c.277A>G
|
XP_016863871.1:p.Ile93Val
|
|
NM_017593.4:c.1165A>G
|
NP_060063.2:p.Ile389Val
|
|
NM_017593.5:c.1165A>G
|
NP_060063.2:p.Ile389Val
|
|
NM_198892.2:c.1165A>G
MANE Select
|
NP_942595.1:p.Ile389Val
|
|