ENST00000695901.1:c.799-753T>C
|
ENSP00000512251.1:n.799-753T>C
|
|
ENST00000695911.1:c.928T>C
|
ENSP00000512262.1:n.928T>C
|
|
ENST00000695912.1:c.1147T>C
|
ENSP00000512263.1:p.Tyr383His
|
|
ENST00000695913.1:c.*1903T>C
|
ENSP00000512264.1:n.*1903T>C
|
|
ENST00000695914.1:c.910T>C
|
ENSP00000512265.1:p.Tyr304His
|
|
ENST00000695918.1:n.378T>C
|
|
|
ENST00000306721.8:c.1150T>C
MANE Select
|
ENSP00000306968.3:p.Tyr384His
|
|
ENST00000306721.7:c.1150T>C
|
ENSP00000306968.3:p.Tyr384His
|
|
ENST00000347703.7:c.913T>C
|
ENSP00000272789.4:p.Tyr305His
|
|
ENST00000410019.3:c.787T>C
|
ENSP00000386833.3:p.Tyr263His
|
|
ENST00000410101.7:c.1018T>C
|
ENSP00000386656.3:p.Tyr340His
|
|
ENST00000467411.5:n.1769-753T>C
|
|
|
ENST00000496441.5:n.1904T>C
|
|
|
NM_031942.4:c.1150T>C
|
NP_114148.3:p.Tyr384His
|
|
NM_145810.2:c.913T>C
|
NP_665809.1:p.Tyr305His
|
|
XM_011511957.1:c.1069T>C
|
XP_011510259.1:p.Tyr357His
|
|
XR_923034.1:n.2048T>C
|
|
|
NM_031942.5:c.1150T>C
MANE Select
|
NP_114148.3:p.Tyr384His
|
|
NM_145810.3:c.913T>C
|
NP_665809.1:p.Tyr305His
|
|