ENST00000389805.9:c.979G>T
MANE Select
|
ENSP00000374455.4:p.Glu327Ter
|
|
ENST00000360718.5:c.727G>T
|
ENSP00000353944.5:p.Glu243Ter
|
|
ENST00000389805.8:c.979G>T
|
ENSP00000374455.4:p.Glu327Ter
|
|
ENST00000510187.5:c.950+369G>T
|
ENSP00000424477.1:n.950+369G>T
|
|
NM_001142298.1:c.727G>T
|
NP_001135770.1:p.Glu243Ter
|
|
NM_001142299.1:c.727G>T
|
NP_001135771.1:p.Glu243Ter
|
|
NM_003900.4:c.979G>T
|
NP_003891.1:p.Glu327Ter
|
|
XM_017010010.1:c.727G>T
|
XP_016865499.1:p.Glu243Ter
|
|
NM_003900.5:c.979G>T
MANE Select
|
NP_003891.1:p.Glu327Ter
|
|
NM_001142298.2:c.727G>T
|
NP_001135770.1:p.Glu243Ter
|
|
NM_001142299.2:c.727G>T
|
NP_001135771.1:p.Glu243Ter
|
|