ENST00000242317.9:c.1826T>G
MANE Select
|
ENSP00000242317.4:p.Ile609Arg
|
|
ENST00000242317.8:c.1826T>G
|
ENSP00000242317.4:p.Ile609Arg
|
|
ENST00000442556.1:c.329+2553T>G
|
|
|
ENST00000470169.5:c.614T>G
|
|
|
ENST00000485580.1:n.402T>G
|
|
|
ENST00000614641.4:c.1838T>G
|
ENSP00000480538.1:p.Ile613Arg
|
|
NM_001281428.1:c.1838T>G
|
NP_001268357.1:p.Ile613Arg
|
|
NM_012144.3:c.1826T>G
|
NP_036276.1:p.Ile609Arg
|
|
XM_006716758.2:c.1295T>G
|
XP_006716821.1:p.Ile432Arg
|
|
XM_011517848.1:c.1580T>G
|
XP_011516150.1:p.Ile527Arg
|
|
XM_006716758.3:c.1295T>G
|
XP_006716821.1:p.Ile432Arg
|
|
XM_011517848.2:c.1580T>G
|
XP_011516150.1:p.Ile527Arg
|
|
XM_017014625.2:c.1568T>G
|
XP_016870114.1:p.Ile523Arg
|
|
XR_002956774.1:n.1929T>G
|
|
|
NM_012144.4:c.1826T>G
MANE Select
|
NP_036276.1:p.Ile609Arg
|
|
NM_001281428.2:c.1838T>G
|
NP_001268357.1:p.Ile613Arg
|
|