ENST00000220616.9:c.8130G>T
MANE Select
|
ENSP00000220616.4:p.Leu2710=
|
|
ENST00000220616.8:c.8130G>T
|
ENSP00000220616.4:p.Leu2710=
|
|
ENST00000519178.5:c.3496G>T
|
|
|
ENST00000519543.5:c.2529G>T
|
ENSP00000430430.1:p.Leu843=
|
|
ENST00000521107.1:c.342G>T
|
ENSP00000430161.1:p.Leu114=
|
|
ENST00000522691.1:n.216G>T
|
|
|
ENST00000523756.5:c.4785G>T
|
|
|
NM_003235.4:c.8130G>T
|
NP_003226.4:p.Leu2710=
|
|
XM_005251038.3:c.7938G>T
|
XP_005251095.1:p.Leu2646=
|
|
XM_006716622.2:c.8067G>T
|
XP_006716685.1:p.Leu2689=
|
|
XM_005251038.4:c.7938G>T
|
XP_005251095.1:p.Leu2646=
|
|
XM_006716622.3:c.8067G>T
|
XP_006716685.1:p.Leu2689=
|
|
XM_017013793.1:c.8064G>T
|
XP_016869282.1:p.Leu2688=
|
|
XM_017013794.1:c.7995G>T
|
XP_016869283.1:p.Leu2665=
|
|
XM_017013795.1:c.7959G>T
|
XP_016869284.1:p.Leu2653=
|
|
XM_017013796.1:c.7911G>T
|
XP_016869285.1:p.Leu2637=
|
|
XM_017013797.1:c.7869G>T
|
XP_016869286.1:p.Leu2623=
|
|
NM_003235.5:c.8130G>T
MANE Select
|
NP_003226.4:p.Leu2710=
|
|