ENST00000340855.11:c.1024C>T
MANE Select
|
ENSP00000339801.6:p.His342Tyr
|
|
ENST00000651111.1:c.391C>T
|
ENSP00000498395.1:p.His131Tyr
|
|
ENST00000340855.10:c.1024C>T
|
ENSP00000339801.6:p.His342Tyr
|
|
ENST00000422081.6:c.391C>T
|
ENSP00000477056.1:p.His131Tyr
|
|
ENST00000441880.1:n.131C>T
|
|
|
NM_000202.6:c.1024C>T
|
NP_000193.1:p.His342Tyr
|
|
NM_001166550.2:c.754C>T
|
NP_001160022.1:p.His252Tyr
|
|
NM_000202.7:c.1024C>T
|
NP_000193.1:p.His342Tyr
|
|
NM_001166550.3:c.754C>T
|
NP_001160022.1:p.His252Tyr
|
|
NM_000202.8:c.1024C>T
MANE Select
|
NP_000193.1:p.His342Tyr
|
|
NM_001166550.4:c.754C>T
|
NP_001160022.1:p.His252Tyr
|
|