ENST00000695901.1:c.798+754G>T
|
ENSP00000512251.1:n.798+754G>T
|
|
ENST00000695911.1:c.877G>T
|
ENSP00000512262.1:n.877G>T
|
|
ENST00000695912.1:c.1096G>T
|
ENSP00000512263.1:p.Asp366Tyr
|
|
ENST00000695913.1:c.*1852G>T
|
ENSP00000512264.1:n.*1852G>T
|
|
ENST00000695914.1:c.859G>T
|
ENSP00000512265.1:p.Asp287Tyr
|
|
ENST00000695918.1:n.327G>T
|
|
|
ENST00000306721.8:c.1099G>T
MANE Select
|
ENSP00000306968.3:p.Asp367Tyr
|
|
ENST00000306721.7:c.1099G>T
|
ENSP00000306968.3:p.Asp367Tyr
|
|
ENST00000347703.7:c.862G>T
|
ENSP00000272789.4:p.Asp288Tyr
|
|
ENST00000410019.3:c.736G>T
|
ENSP00000386833.3:p.Asp246Tyr
|
|
ENST00000410101.7:c.967G>T
|
ENSP00000386656.3:p.Asp323Tyr
|
|
ENST00000467411.5:n.1768+754G>T
|
|
|
ENST00000496441.5:n.1853G>T
|
|
|
NM_031942.4:c.1099G>T
|
NP_114148.3:p.Asp367Tyr
|
|
NM_145810.2:c.862G>T
|
NP_665809.1:p.Asp288Tyr
|
|
XM_011511957.1:c.1018G>T
|
XP_011510259.1:p.Asp340Tyr
|
|
XR_923034.1:n.1997G>T
|
|
|
NM_031942.5:c.1099G>T
MANE Select
|
NP_114148.3:p.Asp367Tyr
|
|
NM_145810.3:c.862G>T
|
NP_665809.1:p.Asp288Tyr
|
|