|
NM_025074.7:c.9466G>T
MANE Select
|
NP_079350.5:p.Glu3156Ter
|
|
ENST00000512123.4:c.9466G>T
MANE Select
|
ENSP00000422834.2:p.Glu3156Ter
|
|
NM_025074.6:c.9466G>T
|
NP_079350.5:p.Glu3156Ter
|
|
ENST00000512123.3:c.9466G>T
|
ENSP00000422834.2:p.Glu3156Ter
|
|
ENST00000682513.1:c.9466G>T
|
ENSP00000508201.1:p.Glu3156Ter
|
|
XM_006714314.1:c.9460G>T
|
XP_006714377.1:p.Glu3154Ter
|
|
XM_006714316.1:c.9238G>T
|
XP_006714379.1:p.Glu3080Ter
|
|
XM_006714316.3:c.9238G>T
|
XP_006714379.1:p.Glu3080Ter
|
|
XM_011532270.1:c.7165G>T
|
XP_011530572.1:p.Glu2389Ter
|
|
XM_011532271.1:c.4354G>T
|
XP_011530573.1:p.Glu1452Ter
|