ENST00000547400.6:c.882G>T
|
ENSP00000446724.2:p.Gln294His
|
|
ENST00000551576.6:c.1152G>T
|
ENSP00000455848.2:p.Gln384His
|
|
ENST00000552678.2:c.1152G>T
|
ENSP00000457394.2:p.Gln384His
|
|
ENST00000388922.9:c.1152G>T
MANE Select
|
ENSP00000373574.4:p.Gln384His
|
|
ENST00000388922.8:c.1152G>T
|
ENSP00000373574.4:p.Gln384His
|
|
ENST00000419526.6:c.630G>T
|
ENSP00000392492.2:p.Gln210His
|
|
ENST00000547632.1:n.427G>T
|
|
|
ENST00000550683.5:c.1194G>T
|
ENSP00000447884.1:p.Gln398His
|
|
ENST00000552678.1:c.157G>T
|
|
|
NM_000020.2:c.1152G>T , LRG_543t1:c.1152G>T
|
NP_000011.2:p.Gln384His
|
|
NM_001077401.1:c.1152G>T
|
NP_001070869.1:p.Gln384His
|
|
XM_005269235.2:c.1152G>T
|
XP_005269292.1:p.Gln384His
|
|
XM_011539008.1:c.882G>T
|
XP_011537310.1:p.Gln294His
|
|
XM_024449279.1:c.363G>T
|
XP_024305047.1:p.Gln121His
|
|
NM_000020.3:c.1152G>T
MANE Select
|
NP_000011.2:p.Gln384His
|
|
NM_001077401.2:c.1152G>T
|
NP_001070869.1:p.Gln384His
|
|