ENST00000402696.9:c.1735G>T
MANE Select
|
ENSP00000385834.3:p.Glu579Ter
|
|
ENST00000402696.7:c.1735G>T
|
ENSP00000385834.3:p.Glu579Ter
|
|
ENST00000461695.1:c.466G>T
|
|
|
ENST00000467842.1:n.2729G>T
|
|
|
NM_001063.3:c.1735G>T
|
NP_001054.1:p.Glu579Ter
|
|
XM_011513100.1:c.1735G>T
|
XP_011511402.1:p.Glu579Ter
|
|
NM_001354703.1:c.1603G>T
|
NP_001341632.1:p.Glu535Ter
|
|
NM_001354704.1:c.1354G>T
|
NP_001341633.1:p.Glu452Ter
|
|
NM_001063.4:c.1735G>T
MANE Select
|
NP_001054.2:p.Glu579Ter
|
|
NM_001354703.2:c.1603G>T
|
NP_001341632.2:p.Glu535Ter
|
|
NM_001354704.2:c.1354G>T
|
NP_001341633.2:p.Glu452Ter
|
|