ENST00000695901.1:c.799-737G>A
|
ENSP00000512251.1:n.799-737G>A
|
|
ENST00000695911.1:c.944G>A
|
ENSP00000512262.1:n.944G>A
|
|
ENST00000695912.1:c.1163G>A
|
ENSP00000512263.1:p.Arg388Lys
|
|
ENST00000695913.1:c.*1919G>A
|
ENSP00000512264.1:n.*1919G>A
|
|
ENST00000695914.1:c.926G>A
|
ENSP00000512265.1:p.Arg309Lys
|
|
ENST00000695918.1:n.394G>A
|
|
|
ENST00000306721.8:c.1166G>A
MANE Select
|
ENSP00000306968.3:p.Arg389Lys
|
|
ENST00000306721.7:c.1166G>A
|
ENSP00000306968.3:p.Arg389Lys
|
|
ENST00000347703.7:c.929G>A
|
ENSP00000272789.4:p.Arg310Lys
|
|
ENST00000410019.3:c.803G>A
|
ENSP00000386833.3:p.Arg268Lys
|
|
ENST00000410101.7:c.1034G>A
|
ENSP00000386656.3:p.Arg345Lys
|
|
ENST00000467411.5:n.1769-737G>A
|
|
|
ENST00000496441.5:n.1920G>A
|
|
|
NM_031942.4:c.1166G>A
|
NP_114148.3:p.Arg389Lys
|
|
NM_145810.2:c.929G>A
|
NP_665809.1:p.Arg310Lys
|
|
XM_011511957.1:c.1085G>A
|
XP_011510259.1:p.Arg362Lys
|
|
XR_923034.1:n.2064G>A
|
|
|
NM_031942.5:c.1166G>A
MANE Select
|
NP_114148.3:p.Arg389Lys
|
|
NM_145810.3:c.929G>A
|
NP_665809.1:p.Arg310Lys
|
|