ENST00000220616.9:c.8055G>T
MANE Select
|
ENSP00000220616.4:p.Trp2685Cys
|
|
ENST00000220616.8:c.8055G>T
|
ENSP00000220616.4:p.Trp2685Cys
|
|
ENST00000519178.5:c.3421G>T
|
|
|
ENST00000519543.5:c.2454G>T
|
ENSP00000430430.1:p.Trp818Cys
|
|
ENST00000521107.1:c.267G>T
|
ENSP00000430161.1:p.Trp89Cys
|
|
ENST00000522691.1:n.141G>T
|
|
|
ENST00000523756.5:c.4710G>T
|
|
|
NM_003235.4:c.8055G>T
|
NP_003226.4:p.Trp2685Cys
|
|
XM_005251038.3:c.7863G>T
|
XP_005251095.1:p.Trp2621Cys
|
|
XM_006716622.2:c.7992G>T
|
XP_006716685.1:p.Trp2664Cys
|
|
XM_005251038.4:c.7863G>T
|
XP_005251095.1:p.Trp2621Cys
|
|
XM_006716622.3:c.7992G>T
|
XP_006716685.1:p.Trp2664Cys
|
|
XM_017013793.1:c.7989G>T
|
XP_016869282.1:p.Trp2663Cys
|
|
XM_017013794.1:c.7920G>T
|
XP_016869283.1:p.Trp2640Cys
|
|
XM_017013795.1:c.7884G>T
|
XP_016869284.1:p.Trp2628Cys
|
|
XM_017013796.1:c.7836G>T
|
XP_016869285.1:p.Trp2612Cys
|
|
XM_017013797.1:c.7794G>T
|
XP_016869286.1:p.Trp2598Cys
|
|
NM_003235.5:c.8055G>T
MANE Select
|
NP_003226.4:p.Trp2685Cys
|
|