ENST00000220616.9:c.8054G>T
MANE Select
|
ENSP00000220616.4:p.Trp2685Leu
|
|
ENST00000220616.8:c.8054G>T
|
ENSP00000220616.4:p.Trp2685Leu
|
|
ENST00000519178.5:c.3420G>T
|
|
|
ENST00000519543.5:c.2453G>T
|
ENSP00000430430.1:p.Trp818Leu
|
|
ENST00000521107.1:c.266G>T
|
ENSP00000430161.1:p.Trp89Leu
|
|
ENST00000522691.1:n.140G>T
|
|
|
ENST00000523756.5:c.4709G>T
|
|
|
NM_003235.4:c.8054G>T
|
NP_003226.4:p.Trp2685Leu
|
|
XM_005251038.3:c.7862G>T
|
XP_005251095.1:p.Trp2621Leu
|
|
XM_006716622.2:c.7991G>T
|
XP_006716685.1:p.Trp2664Leu
|
|
XM_005251038.4:c.7862G>T
|
XP_005251095.1:p.Trp2621Leu
|
|
XM_006716622.3:c.7991G>T
|
XP_006716685.1:p.Trp2664Leu
|
|
XM_017013793.1:c.7988G>T
|
XP_016869282.1:p.Trp2663Leu
|
|
XM_017013794.1:c.7919G>T
|
XP_016869283.1:p.Trp2640Leu
|
|
XM_017013795.1:c.7883G>T
|
XP_016869284.1:p.Trp2628Leu
|
|
XM_017013796.1:c.7835G>T
|
XP_016869285.1:p.Trp2612Leu
|
|
XM_017013797.1:c.7793G>T
|
XP_016869286.1:p.Trp2598Leu
|
|
NM_003235.5:c.8054G>T
MANE Select
|
NP_003226.4:p.Trp2685Leu
|
|