ENST00000695901.1:c.798+743G>T
|
ENSP00000512251.1:n.798+743G>T
|
|
ENST00000695911.1:c.866G>T
|
ENSP00000512262.1:n.866G>T
|
|
ENST00000695912.1:c.1085G>T
|
ENSP00000512263.1:p.Cys362Phe
|
|
ENST00000695913.1:c.*1841G>T
|
ENSP00000512264.1:n.*1841G>T
|
|
ENST00000695914.1:c.848G>T
|
ENSP00000512265.1:p.Cys283Phe
|
|
ENST00000695918.1:n.316G>T
|
|
|
ENST00000306721.8:c.1088G>T
MANE Select
|
ENSP00000306968.3:p.Cys363Phe
|
|
ENST00000306721.7:c.1088G>T
|
ENSP00000306968.3:p.Cys363Phe
|
|
ENST00000347703.7:c.851G>T
|
ENSP00000272789.4:p.Cys284Phe
|
|
ENST00000410019.3:c.725G>T
|
ENSP00000386833.3:p.Cys242Phe
|
|
ENST00000410101.7:c.956G>T
|
ENSP00000386656.3:p.Cys319Phe
|
|
ENST00000467411.5:n.1768+743G>T
|
|
|
ENST00000496441.5:n.1842G>T
|
|
|
NM_031942.4:c.1088G>T
|
NP_114148.3:p.Cys363Phe
|
|
NM_145810.2:c.851G>T
|
NP_665809.1:p.Cys284Phe
|
|
XM_011511957.1:c.1007G>T
|
XP_011510259.1:p.Cys336Phe
|
|
XR_923034.1:n.1986G>T
|
|
|
NM_031942.5:c.1088G>T
MANE Select
|
NP_114148.3:p.Cys363Phe
|
|
NM_145810.3:c.851G>T
|
NP_665809.1:p.Cys284Phe
|
|