ENST00000247933.9:c.678C>A
|
ENSP00000247933.4:p.His226Gln
|
|
ENST00000514224.2:c.678C>A
MANE Select
|
ENSP00000425081.2:p.His226Gln
|
|
ENST00000652070.1:n.734C>A
|
|
|
ENST00000247933.8:c.678C>A
|
ENSP00000247933.4:p.His226Gln
|
|
ENST00000502910.5:c.537C>A
|
ENSP00000422952.1:p.His179Gln
|
|
ENST00000509948.5:c.471C>A
|
ENSP00000424227.1:p.His157Gln
|
|
ENST00000514192.5:c.495C>A
|
ENSP00000423685.1:p.His165Gln
|
|
ENST00000514224.1:c.282C>A
|
ENSP00000425081.1:p.His94Gln
|
|
ENST00000514698.5:n.578C>A
|
|
|
NM_000203.4:c.678C>A
|
NP_000194.2:p.His226Gln
|
|
NR_110313.1:n.766C>A
|
|
|
XM_006713882.2:c.282C>A
|
XP_006713945.1:p.His94Gln
|
|
XM_011513459.1:c.537C>A
|
XP_011511761.1:p.His179Gln
|
|
XM_011513460.1:c.537C>A
|
XP_011511762.1:p.His179Gln
|
|
XM_011513461.1:c.471C>A
|
XP_011511763.1:p.His157Gln
|
|
XM_011513462.1:c.390C>A
|
XP_011511764.1:p.His130Gln
|
|
XM_011513463.1:c.390C>A
|
XP_011511765.1:p.His130Gln
|
|
XR_924947.1:n.747C>A
|
|
|
NM_000203.5:c.678C>A
MANE Select
|
NP_000194.2:p.His226Gln
|
|
NM_001363576.1:c.282C>A
|
NP_001350505.1:p.His94Gln
|
|
XM_011513461.2:c.471C>A
|
XP_011511763.1:p.His157Gln
|
|
XM_017008163.1:c.-283C>A
|
XP_016863652.1:n.-283C>A
|
|