ENST00000474627.8:c.566G>A
MANE Select
|
ENSP00000417190.2:p.Arg189Gln
|
|
ENST00000444058.1:c.566G>A
|
ENSP00000397198.1:p.Arg189Gln
|
|
ENST00000462733.5:c.*34-557G>A
|
ENSP00000463920.1:n.*34-557G>A
|
|
ENST00000469327.5:n.234G>A
|
|
|
ENST00000474627.7:c.566G>A
|
ENSP00000417190.2:p.Arg189Gln
|
|
ENST00000488753.1:n.361G>A
|
|
|
ENST00000496852.5:n.1071G>A
|
|
|
ENST00000581698.1:c.48+2829G>A
|
|
|
ENST00000584205.5:c.*33+2829G>A
|
ENSP00000462899.1:n.*33+2829G>A
|
|
ENST00000585101.5:c.*33+2829G>A
|
ENSP00000463861.1:n.*33+2829G>A
|
|
NM_145691.3:c.566G>A
|
NP_663729.1:p.Arg189Gln
|
|
XM_005256848.2:c.566G>A
|
XP_005256905.1:p.Arg189Gln
|
|
XM_011524062.1:c.566G>A
|
XP_011522364.1:p.Arg189Gln
|
|
XM_011524063.1:c.566G>A
|
XP_011522365.1:p.Arg189Gln
|
|
XM_011524064.1:c.266G>A
|
XP_011522366.1:p.Arg89Gln
|
|
XM_011524065.1:c.566G>A
|
XP_011522367.1:p.Arg189Gln
|
|
XM_011524066.1:c.29G>A
|
XP_011522368.1:p.Arg10Gln
|
|
XR_934116.1:n.722G>A
|
|
|
XM_005256848.4:c.566G>A
|
XP_005256905.1:p.Arg189Gln
|
|
XM_011524065.2:c.566G>A
|
XP_011522367.1:p.Arg189Gln
|
|
XM_017025302.1:c.266G>A
|
XP_016880791.1:p.Arg89Gln
|
|
XM_017025303.1:c.266G>A
|
XP_016880792.1:p.Arg89Gln
|
|
XR_001752677.2:n.721G>A
|
|
|
NM_145691.4:c.566G>A
MANE Select
|
NP_663729.1:p.Arg189Gln
|
|