ENST00000684880.1:c.*27G>T
|
ENSP00000510280.1:n.*27G>T
|
|
ENST00000689310.1:c.391G>T
|
ENSP00000510438.1:p.Glu131Ter
|
|
ENST00000692630.1:n.569G>T
|
|
|
ENST00000370818.8:c.439G>T
MANE Select
|
ENSP00000359854.3:p.Glu147Ter
|
|
ENST00000394299.7:c.439G>T
|
ENSP00000377836.2:p.Glu147Ter
|
|
ENST00000370818.7:c.439G>T
|
ENSP00000359854.3:p.Glu147Ter
|
|
ENST00000394299.6:c.439G>T
|
ENSP00000377836.2:p.Glu147Ter
|
|
ENST00000631057.2:c.277G>T
|
ENSP00000486325.1:p.Glu93Ter
|
|
NM_001164617.1:c.439G>T
|
NP_001158089.1:p.Glu147Ter
|
|
NM_001164618.1:c.391G>T
|
NP_001158090.1:p.Glu131Ter
|
|
NM_001164619.1:c.277G>T
|
NP_001158091.1:p.Glu93Ter
|
|
NM_004484.3:c.439G>T , LRG_505t1:c.439G>T
|
NP_004475.1:p.Glu147Ter
|
|
XM_017029413.2:c.439G>T
|
XP_016884902.1:p.Glu147Ter
|
|
NM_001164617.2:c.439G>T
|
NP_001158089.1:p.Glu147Ter
|
|
NM_001164618.2:c.391G>T
|
NP_001158090.1:p.Glu131Ter
|
|
NM_001164619.2:c.277G>T
|
NP_001158091.1:p.Glu93Ter
|
|
NM_004484.4:c.439G>T
MANE Select
|
NP_004475.1:p.Glu147Ter
|
|