ENST00000695901.1:c.798+777G>C
|
ENSP00000512251.1:n.798+777G>C
|
|
ENST00000695911.1:c.900G>C
|
ENSP00000512262.1:n.900G>C
|
|
ENST00000695912.1:c.1119G>C
|
ENSP00000512263.1:p.Gln373His
|
|
ENST00000695913.1:c.*1875G>C
|
ENSP00000512264.1:n.*1875G>C
|
|
ENST00000695914.1:c.882G>C
|
ENSP00000512265.1:p.Gln294His
|
|
ENST00000695918.1:n.350G>C
|
|
|
ENST00000306721.8:c.1122G>C
MANE Select
|
ENSP00000306968.3:p.Gln374His
|
|
ENST00000306721.7:c.1122G>C
|
ENSP00000306968.3:p.Gln374His
|
|
ENST00000347703.7:c.885G>C
|
ENSP00000272789.4:p.Gln295His
|
|
ENST00000410019.3:c.759G>C
|
ENSP00000386833.3:p.Gln253His
|
|
ENST00000410101.7:c.990G>C
|
ENSP00000386656.3:p.Gln330His
|
|
ENST00000467411.5:n.1768+777G>C
|
|
|
ENST00000496441.5:n.1876G>C
|
|
|
NM_031942.4:c.1122G>C
|
NP_114148.3:p.Gln374His
|
|
NM_145810.2:c.885G>C
|
NP_665809.1:p.Gln295His
|
|
XM_011511957.1:c.1041G>C
|
XP_011510259.1:p.Gln347His
|
|
XR_923034.1:n.2020G>C
|
|
|
NM_031942.5:c.1122G>C
MANE Select
|
NP_114148.3:p.Gln374His
|
|
NM_145810.3:c.885G>C
|
NP_665809.1:p.Gln295His
|
|