ENST00000695901.1:c.798+778T>G
|
ENSP00000512251.1:n.798+778T>G
|
|
ENST00000695911.1:c.901T>G
|
ENSP00000512262.1:n.901T>G
|
|
ENST00000695912.1:c.1120T>G
|
ENSP00000512263.1:p.Phe374Val
|
|
ENST00000695913.1:c.*1876T>G
|
ENSP00000512264.1:n.*1876T>G
|
|
ENST00000695914.1:c.883T>G
|
ENSP00000512265.1:p.Phe295Val
|
|
ENST00000695918.1:n.351T>G
|
|
|
ENST00000306721.8:c.1123T>G
MANE Select
|
ENSP00000306968.3:p.Phe375Val
|
|
ENST00000306721.7:c.1123T>G
|
ENSP00000306968.3:p.Phe375Val
|
|
ENST00000347703.7:c.886T>G
|
ENSP00000272789.4:p.Phe296Val
|
|
ENST00000410019.3:c.760T>G
|
ENSP00000386833.3:p.Phe254Val
|
|
ENST00000410101.7:c.991T>G
|
ENSP00000386656.3:p.Phe331Val
|
|
ENST00000467411.5:n.1768+778T>G
|
|
|
ENST00000496441.5:n.1877T>G
|
|
|
NM_031942.4:c.1123T>G
|
NP_114148.3:p.Phe375Val
|
|
NM_145810.2:c.886T>G
|
NP_665809.1:p.Phe296Val
|
|
XM_011511957.1:c.1042T>G
|
XP_011510259.1:p.Phe348Val
|
|
XR_923034.1:n.2021T>G
|
|
|
NM_031942.5:c.1123T>G
MANE Select
|
NP_114148.3:p.Phe375Val
|
|
NM_145810.3:c.886T>G
|
NP_665809.1:p.Phe296Val
|
|