|
NM_025074.7:c.6726G>A
MANE Select
|
NP_079350.5:p.Gln2242=
|
|
ENST00000512123.4:c.6726G>A
MANE Select
|
ENSP00000422834.2:p.Gln2242=
|
|
NM_025074.6:c.6726G>A
|
NP_079350.5:p.Gln2242=
|
|
ENST00000512123.3:c.6726G>A
|
ENSP00000422834.2:p.Gln2242=
|
|
ENST00000682513.1:c.6726G>A
|
ENSP00000508201.1:p.Gln2242=
|
|
XM_006714314.1:c.6720G>A
|
XP_006714377.1:p.Gln2240=
|
|
XM_006714316.1:c.6726G>A
|
XP_006714379.1:p.Gln2242=
|
|
XM_006714316.3:c.6726G>A
|
XP_006714379.1:p.Gln2242=
|
|
XM_011532270.1:c.4425G>A
|
XP_011530572.1:p.Gln1475=
|
|
XM_011532271.1:c.1614G>A
|
XP_011530573.1:p.Gln538=
|