NM_025074.7:c.8602C=
MANE Select
|
NP_079350.5:p.Gln2868=
|
ENST00000512123.4:c.8602C=
MANE Select
|
ENSP00000422834.2:p.Gln2868=
|
NM_025074.6:c.8602C=
|
NP_079350.5:p.Gln2868=
|
ENST00000512123.3:c.8602C=
|
ENSP00000422834.2:p.Gln2868=
|
ENST00000682513.1:c.8602C=
|
ENSP00000508201.1:p.Gln2868=
|
XM_006714314.1:c.8596C=
|
XP_006714377.1:p.Gln2866=
|
XM_006714316.1:c.8374C=
|
XP_006714379.1:p.Gln2792=
|
XM_006714316.3:c.8374C=
|
XP_006714379.1:p.Gln2792=
|
XM_011532270.1:c.6301C=
|
XP_011530572.1:p.Gln2101=
|
XM_011532271.1:c.3490C=
|
XP_011530573.1:p.Gln1164=
|