|
NM_000081.4:c.10813G>T
MANE Select
|
NP_000072.2:p.Glu3605Ter
|
|
ENST00000389793.7:c.10813G>T
MANE Select
|
ENSP00000374443.2:p.Glu3605Ter
|
|
NM_000081.3:c.10813G>T , LRG_143t1:c.10813G>T
|
NP_000072.2:p.Glu3605Ter
|
|
NM_001301365.1:c.10813G>T , LRG_143t2:c.10813G>T
|
NP_001288294.1:p.Glu3605Ter
|
|
ENST00000389793.6:c.10813G>T
|
ENSP00000374443.2:p.Glu3605Ter
|
|
ENST00000389794.7:c.*6237G>T
|
ENSP00000374444.4:n.*6237G>T
|
|
ENST00000462376.2:n.2223G>T
|
|
|
ENST00000473037.5:n.5803G>T
|
|
|
ENST00000697178.1:c.*6508G>T
|
ENSP00000513163.1:n.*6508G>T
|
|
ENST00000697235.1:c.1363G>T
|
ENSP00000513202.1:p.Glu455Ter
|
|
ENST00000697236.1:c.4277G>T
|
ENSP00000513203.1:n.4277G>T
|
|
ENST00000697237.1:c.1524G>T
|
|
|
ENST00000697239.1:n.207G>T
|
|
|
ENST00000697240.1:c.2947G>T
|
ENSP00000513205.1:p.Glu983Ter
|
|
XM_011544031.1:c.10975G>T
|
XP_011542333.1:p.Glu3659Ter
|
|
XM_011544032.1:c.10975G>T
|
XP_011542334.1:p.Glu3659Ter
|
|
XM_011544033.1:c.10975G>T
|
XP_011542335.1:p.Glu3659Ter
|
|
XM_011544033.2:c.10975G>T
|
XP_011542335.1:p.Glu3659Ter
|
|
XM_011544034.1:c.10837G>T
|
XP_011542336.1:p.Glu3613Ter
|
|
XM_011544036.1:c.8638G>T
|
XP_011542338.1:p.Glu2880Ter
|
|
XM_011544036.2:c.8638G>T
|
XP_011542338.1:p.Glu2880Ter
|
|
XM_017000150.1:c.10744G>T
|
XP_016855639.1:p.Glu3582Ter
|