ENST00000547400.6:c.841G>T
|
ENSP00000446724.2:p.Gly281Cys
|
|
ENST00000551576.6:c.1111G>T
|
ENSP00000455848.2:p.Gly371Cys
|
|
ENST00000552678.2:c.1111G>T
|
ENSP00000457394.2:p.Gly371Cys
|
|
ENST00000388922.9:c.1111G>T
MANE Select
|
ENSP00000373574.4:p.Gly371Cys
|
|
ENST00000388922.8:c.1111G>T
|
ENSP00000373574.4:p.Gly371Cys
|
|
ENST00000419526.6:c.589G>T
|
ENSP00000392492.2:p.Gly197Cys
|
|
ENST00000547632.1:n.386G>T
|
|
|
ENST00000550683.5:c.1153G>T
|
ENSP00000447884.1:p.Gly385Cys
|
|
ENST00000552678.1:c.116G>T
|
|
|
NM_000020.2:c.1111G>T , LRG_543t1:c.1111G>T
|
NP_000011.2:p.Gly371Cys
|
|
NM_001077401.1:c.1111G>T
|
NP_001070869.1:p.Gly371Cys
|
|
XM_005269235.2:c.1111G>T
|
XP_005269292.1:p.Gly371Cys
|
|
XM_011539008.1:c.841G>T
|
XP_011537310.1:p.Gly281Cys
|
|
XM_024449279.1:c.322G>T
|
XP_024305047.1:p.Gly108Cys
|
|
NM_000020.3:c.1111G>T
MANE Select
|
NP_000011.2:p.Gly371Cys
|
|
NM_001077401.2:c.1111G>T
|
NP_001070869.1:p.Gly371Cys
|
|