|
NM_016216.4:c.49T>C
MANE Select
|
NP_057300.2:p.Tyr17His
|
|
ENST00000260803.9:c.49T>C
MANE Select
|
ENSP00000260803.4:p.Tyr17His
|
|
NM_016216.3:c.49T>C
|
NP_057300.2:p.Tyr17His
|
|
ENST00000260803.8:c.49T>C
|
ENSP00000260803.4:p.Tyr17His
|
|
ENST00000463982.2:n.120T>C
|
|
|
ENST00000463982.3:n.195T>C
|
|
|
ENST00000477557.3:c.49T>C
|
ENSP00000417262.3:p.Tyr17His
|
|
ENST00000698922.1:c.49T>C
|
ENSP00000514033.1:p.Tyr17His
|
|
ENST00000698923.1:c.49T>C
|
ENSP00000514034.1:p.Tyr17His
|
|
ENST00000698924.1:c.49T>C
|
ENSP00000514035.1:p.Tyr17His
|
|
ENST00000698925.1:c.49T>C
|
ENSP00000514036.1:p.Tyr17His
|