ENST00000695901.1:c.798+452T>G
|
ENSP00000512251.1:n.798+452T>G
|
|
ENST00000695911.1:c.814-239T>G
|
ENSP00000512262.1:n.814-239T>G
|
|
ENST00000695912.1:c.1033-239T>G
|
ENSP00000512263.1:n.1033-239T>G
|
|
ENST00000695913.1:c.*1550T>G
|
ENSP00000512264.1:n.*1550T>G
|
|
ENST00000695914.1:c.796-239T>G
|
ENSP00000512265.1:n.796-239T>G
|
|
ENST00000695918.1:n.264-239T>G
|
|
|
ENST00000306721.8:c.1036-239T>G
MANE Select
|
ENSP00000306968.3:n.1036-239T>G
|
|
ENST00000306721.7:c.1036-239T>G
|
ENSP00000306968.3:n.1036-239T>G
|
|
ENST00000347703.7:c.799-239T>G
|
ENSP00000272789.4:n.799-239T>G
|
|
ENST00000410019.3:c.673-239T>G
|
ENSP00000386833.3:n.673-239T>G
|
|
ENST00000410101.7:c.904-239T>G
|
ENSP00000386656.3:n.904-239T>G
|
|
ENST00000467411.5:n.1768+452T>G
|
|
|
ENST00000496441.5:n.1790-239T>G
|
|
|
NM_031942.4:c.1036-239T>G
|
NP_114148.3:n.1036-239T>G
|
|
NM_145810.2:c.799-239T>G
|
NP_665809.1:n.799-239T>G
|
|
XM_011511957.1:c.955-239T>G
|
XP_011510259.1:n.955-239T>G
|
|
XR_923034.1:n.1934-239T>G
|
|
|
NM_031942.5:c.1036-239T>G
MANE Select
|
NP_114148.3:n.1036-239T>G
|
|
NM_145810.3:c.799-239T>G
|
NP_665809.1:n.799-239T>G
|
|