ENST00000220616.9:c.8095G>T
MANE Select
|
ENSP00000220616.4:p.Glu2699Ter
|
|
ENST00000220616.8:c.8095G>T
|
ENSP00000220616.4:p.Glu2699Ter
|
|
ENST00000519178.5:c.3461G>T
|
|
|
ENST00000519543.5:c.2494G>T
|
ENSP00000430430.1:p.Glu832Ter
|
|
ENST00000521107.1:c.307G>T
|
ENSP00000430161.1:p.Glu103Ter
|
|
ENST00000522691.1:n.181G>T
|
|
|
ENST00000523756.5:c.4750G>T
|
|
|
NM_003235.4:c.8095G>T
|
NP_003226.4:p.Glu2699Ter
|
|
XM_005251038.3:c.7903G>T
|
XP_005251095.1:p.Glu2635Ter
|
|
XM_006716622.2:c.8032G>T
|
XP_006716685.1:p.Glu2678Ter
|
|
XM_005251038.4:c.7903G>T
|
XP_005251095.1:p.Glu2635Ter
|
|
XM_006716622.3:c.8032G>T
|
XP_006716685.1:p.Glu2678Ter
|
|
XM_017013793.1:c.8029G>T
|
XP_016869282.1:p.Glu2677Ter
|
|
XM_017013794.1:c.7960G>T
|
XP_016869283.1:p.Glu2654Ter
|
|
XM_017013795.1:c.7924G>T
|
XP_016869284.1:p.Glu2642Ter
|
|
XM_017013796.1:c.7876G>T
|
XP_016869285.1:p.Glu2626Ter
|
|
XM_017013797.1:c.7834G>T
|
XP_016869286.1:p.Glu2612Ter
|
|
NM_003235.5:c.8095G>T
MANE Select
|
NP_003226.4:p.Glu2699Ter
|
|