ENST00000394867.9:n.1550C>G
|
|
|
ENST00000688002.1:n.3262C>G
|
|
|
ENST00000688751.1:n.247C>G
|
|
|
ENST00000689792.1:n.1015C>G
|
|
|
ENST00000262948.10:c.1111C>G
MANE Select
|
ENSP00000262948.4:p.Arg371Gly
|
|
ENST00000262948.9:c.1111C>G
|
ENSP00000262948.3:p.Arg371Gly
|
|
ENST00000394867.8:c.820C>G
|
ENSP00000378336.1:p.Arg274Gly
|
|
ENST00000597263.5:n.296C>G
|
|
|
ENST00000599021.1:c.221C>G
|
|
|
ENST00000600584.5:n.2560C>G
|
|
|
ENST00000601786.5:n.1412C>G
|
|
|
NM_030662.3:c.1111C>G , LRG_750t1:c.1111C>G
|
NP_109587.1:p.Arg371Gly
|
|
XM_006722799.2:c.832C>G
|
XP_006722862.1:p.Arg278Gly
|
|
XM_011528133.1:c.541C>G
|
XP_011526435.1:p.Arg181Gly
|
|
NM_030662.4:c.1111C>G
MANE Select
|
NP_109587.1:p.Arg371Gly
|
|