ENST00000394867.9:n.1492C>G
|
|
|
ENST00000688002.1:n.3204C>G
|
|
|
ENST00000688751.1:n.189C>G
|
|
|
ENST00000689792.1:n.957C>G
|
|
|
ENST00000262948.10:c.1053C>G
MANE Select
|
ENSP00000262948.4:p.Ile351Met
|
|
ENST00000262948.9:c.1053C>G
|
ENSP00000262948.3:p.Ile351Met
|
|
ENST00000394867.8:c.762C>G
|
ENSP00000378336.1:p.Ile254Met
|
|
ENST00000597263.5:n.238C>G
|
|
|
ENST00000599021.1:c.163C>G
|
|
|
ENST00000600584.5:n.2502C>G
|
|
|
ENST00000601786.5:n.1354C>G
|
|
|
NM_030662.3:c.1053C>G , LRG_750t1:c.1053C>G
|
NP_109587.1:p.Ile351Met
|
|
XM_006722799.2:c.774C>G
|
XP_006722862.1:p.Ile258Met
|
|
XM_011528133.1:c.483C>G
|
XP_011526435.1:p.Ile161Met
|
|
NM_030662.4:c.1053C>G
MANE Select
|
NP_109587.1:p.Ile351Met
|
|