ENST00000695901.1:c.798+717G>C
|
ENSP00000512251.1:n.798+717G>C
|
|
ENST00000695911.1:c.840G>C
|
ENSP00000512262.1:n.840G>C
|
|
ENST00000695912.1:c.1059G>C
|
ENSP00000512263.1:p.Gln353His
|
|
ENST00000695913.1:c.*1815G>C
|
ENSP00000512264.1:n.*1815G>C
|
|
ENST00000695914.1:c.822G>C
|
ENSP00000512265.1:p.Gln274His
|
|
ENST00000695918.1:n.290G>C
|
|
|
ENST00000306721.8:c.1062G>C
MANE Select
|
ENSP00000306968.3:p.Gln354His
|
|
ENST00000306721.7:c.1062G>C
|
ENSP00000306968.3:p.Gln354His
|
|
ENST00000347703.7:c.825G>C
|
ENSP00000272789.4:p.Gln275His
|
|
ENST00000410019.3:c.699G>C
|
ENSP00000386833.3:p.Gln233His
|
|
ENST00000410101.7:c.930G>C
|
ENSP00000386656.3:p.Gln310His
|
|
ENST00000467411.5:n.1768+717G>C
|
|
|
ENST00000496441.5:n.1816G>C
|
|
|
NM_031942.4:c.1062G>C
|
NP_114148.3:p.Gln354His
|
|
NM_145810.2:c.825G>C
|
NP_665809.1:p.Gln275His
|
|
XM_011511957.1:c.981G>C
|
XP_011510259.1:p.Gln327His
|
|
XR_923034.1:n.1960G>C
|
|
|
NM_031942.5:c.1062G>C
MANE Select
|
NP_114148.3:p.Gln354His
|
|
NM_145810.3:c.825G>C
|
NP_665809.1:p.Gln275His
|
|