ENST00000547400.6:c.606G>T
|
ENSP00000446724.2:p.Gln202His
|
|
ENST00000551576.6:c.876G>T
|
ENSP00000455848.2:p.Gln292His
|
|
ENST00000552678.2:c.876G>T
|
ENSP00000457394.2:p.Gln292His
|
|
ENST00000388922.9:c.876G>T
MANE Select
|
ENSP00000373574.4:p.Gln292His
|
|
ENST00000388922.8:c.876G>T
|
ENSP00000373574.4:p.Gln292His
|
|
ENST00000419526.6:c.354G>T
|
ENSP00000392492.2:p.Gln118His
|
|
ENST00000550683.5:c.918G>T
|
ENSP00000447884.1:p.Gln306His
|
|
NM_000020.2:c.876G>T , LRG_543t1:c.876G>T
|
NP_000011.2:p.Gln292His
|
|
NM_001077401.1:c.876G>T
|
NP_001070869.1:p.Gln292His
|
|
XM_005269235.2:c.876G>T
|
XP_005269292.1:p.Gln292His
|
|
XM_011539008.1:c.606G>T
|
XP_011537310.1:p.Gln202His
|
|
XM_024449279.1:c.87G>T
|
XP_024305047.1:p.Gln29His
|
|
NM_000020.3:c.876G>T
MANE Select
|
NP_000011.2:p.Gln292His
|
|
NM_001077401.2:c.876G>T
|
NP_001070869.1:p.Gln292His
|
|