ENST00000695901.1:c.798+771A>C
|
ENSP00000512251.1:n.798+771A>C
|
|
ENST00000695911.1:c.894A>C
|
ENSP00000512262.1:n.894A>C
|
|
ENST00000695912.1:c.1113A>C
|
ENSP00000512263.1:p.Arg371=
|
|
ENST00000695913.1:c.*1869A>C
|
ENSP00000512264.1:n.*1869A>C
|
|
ENST00000695914.1:c.876A>C
|
ENSP00000512265.1:p.Arg292=
|
|
ENST00000695918.1:n.344A>C
|
|
|
ENST00000306721.8:c.1116A>C
MANE Select
|
ENSP00000306968.3:p.Arg372=
|
|
ENST00000306721.7:c.1116A>C
|
ENSP00000306968.3:p.Arg372=
|
|
ENST00000347703.7:c.879A>C
|
ENSP00000272789.4:p.Arg293=
|
|
ENST00000410019.3:c.753A>C
|
ENSP00000386833.3:p.Arg251=
|
|
ENST00000410101.7:c.984A>C
|
ENSP00000386656.3:p.Arg328=
|
|
ENST00000467411.5:n.1768+771A>C
|
|
|
ENST00000496441.5:n.1870A>C
|
|
|
NM_031942.4:c.1116A>C
|
NP_114148.3:p.Arg372=
|
|
NM_145810.2:c.879A>C
|
NP_665809.1:p.Arg293=
|
|
XM_011511957.1:c.1035A>C
|
XP_011510259.1:p.Arg345=
|
|
XR_923034.1:n.2014A>C
|
|
|
NM_031942.5:c.1116A>C
MANE Select
|
NP_114148.3:p.Arg372=
|
|
NM_145810.3:c.879A>C
|
NP_665809.1:p.Arg293=
|
|