ENST00000695901.1:c.798+726T>C
|
ENSP00000512251.1:n.798+726T>C
|
|
ENST00000695911.1:c.849T>C
|
ENSP00000512262.1:n.849T>C
|
|
ENST00000695912.1:c.1068T>C
|
ENSP00000512263.1:p.Ile356=
|
|
ENST00000695913.1:c.*1824T>C
|
ENSP00000512264.1:n.*1824T>C
|
|
ENST00000695914.1:c.831T>C
|
ENSP00000512265.1:p.Ile277=
|
|
ENST00000695918.1:n.299T>C
|
|
|
ENST00000306721.8:c.1071T>C
MANE Select
|
ENSP00000306968.3:p.Ile357=
|
|
ENST00000306721.7:c.1071T>C
|
ENSP00000306968.3:p.Ile357=
|
|
ENST00000347703.7:c.834T>C
|
ENSP00000272789.4:p.Ile278=
|
|
ENST00000410019.3:c.708T>C
|
ENSP00000386833.3:p.Ile236=
|
|
ENST00000410101.7:c.939T>C
|
ENSP00000386656.3:p.Ile313=
|
|
ENST00000467411.5:n.1768+726T>C
|
|
|
ENST00000496441.5:n.1825T>C
|
|
|
NM_031942.4:c.1071T>C
|
NP_114148.3:p.Ile357=
|
|
NM_145810.2:c.834T>C
|
NP_665809.1:p.Ile278=
|
|
XM_011511957.1:c.990T>C
|
XP_011510259.1:p.Ile330=
|
|
XR_923034.1:n.1969T>C
|
|
|
NM_031942.5:c.1071T>C
MANE Select
|
NP_114148.3:p.Ile357=
|
|
NM_145810.3:c.834T>C
|
NP_665809.1:p.Ile278=
|
|