ENST00000682513.1:c.8833G>A
|
ENSP00000508201.1:p.Gly2945Arg
|
|
ENST00000512123.4:c.8833G>A
MANE Select
|
ENSP00000422834.2:p.Gly2945Arg
|
|
ENST00000512123.3:c.8833G>A
|
ENSP00000422834.2:p.Gly2945Arg
|
|
NM_025074.6:c.8833G>A
|
NP_079350.5:p.Gly2945Arg
|
|
XM_006714314.1:c.8827G>A
|
XP_006714377.1:p.Gly2943Arg
|
|
XM_006714316.1:c.8605G>A
|
XP_006714379.1:p.Gly2869Arg
|
|
XM_011532270.1:c.6532G>A
|
XP_011530572.1:p.Gly2178Arg
|
|
XM_011532271.1:c.3721G>A
|
XP_011530573.1:p.Gly1241Arg
|
|
XM_006714316.3:c.8605G>A
|
XP_006714379.1:p.Gly2869Arg
|
|
NM_025074.7:c.8833G>A
MANE Select
|
NP_079350.5:p.Gly2945Arg
|
|