ENST00000547400.6:c.574C>T
|
ENSP00000446724.2:p.His192Tyr
|
|
ENST00000551576.6:c.844C>T
|
ENSP00000455848.2:p.His282Tyr
|
|
ENST00000552678.2:c.844C>T
|
ENSP00000457394.2:p.His282Tyr
|
|
ENST00000388922.9:c.844C>T
MANE Select
|
ENSP00000373574.4:p.His282Tyr
|
|
ENST00000388922.8:c.844C>T
|
ENSP00000373574.4:p.His282Tyr
|
|
ENST00000419526.6:c.322C>T
|
ENSP00000392492.2:p.His108Tyr
|
|
ENST00000550683.5:c.886C>T
|
ENSP00000447884.1:p.His296Tyr
|
|
NM_000020.2:c.844C>T , LRG_543t1:c.844C>T
|
NP_000011.2:p.His282Tyr
|
|
NM_001077401.1:c.844C>T
|
NP_001070869.1:p.His282Tyr
|
|
XM_005269235.2:c.844C>T
|
XP_005269292.1:p.His282Tyr
|
|
XM_011539008.1:c.574C>T
|
XP_011537310.1:p.His192Tyr
|
|
XM_024449279.1:c.55C>T
|
XP_024305047.1:p.His19Tyr
|
|
NM_000020.3:c.844C>T
MANE Select
|
NP_000011.2:p.His282Tyr
|
|
NM_001077401.2:c.844C>T
|
NP_001070869.1:p.His282Tyr
|
|