ENST00000547400.6:c.835A>G
|
ENSP00000446724.2:p.Arg279Gly
|
|
ENST00000551576.6:c.1105A>G
|
ENSP00000455848.2:p.Arg369Gly
|
|
ENST00000552678.2:c.1105A>G
|
ENSP00000457394.2:p.Arg369Gly
|
|
ENST00000388922.9:c.1105A>G
MANE Select
|
ENSP00000373574.4:p.Arg369Gly
|
|
ENST00000388922.8:c.1105A>G
|
ENSP00000373574.4:p.Arg369Gly
|
|
ENST00000419526.6:c.583A>G
|
ENSP00000392492.2:p.Arg195Gly
|
|
ENST00000547632.1:n.380A>G
|
|
|
ENST00000550683.5:c.1147A>G
|
ENSP00000447884.1:p.Arg383Gly
|
|
ENST00000552678.1:c.110A>G
|
|
|
NM_000020.2:c.1105A>G , LRG_543t1:c.1105A>G
|
NP_000011.2:p.Arg369Gly
|
|
NM_001077401.1:c.1105A>G
|
NP_001070869.1:p.Arg369Gly
|
|
XM_005269235.2:c.1105A>G
|
XP_005269292.1:p.Arg369Gly
|
|
XM_011539008.1:c.835A>G
|
XP_011537310.1:p.Arg279Gly
|
|
XM_024449279.1:c.316A>G
|
XP_024305047.1:p.Arg106Gly
|
|
NM_000020.3:c.1105A>G
MANE Select
|
NP_000011.2:p.Arg369Gly
|
|
NM_001077401.2:c.1105A>G
|
NP_001070869.1:p.Arg369Gly
|
|