ENST00000352511.5:c.1183G>T
MANE Select
|
ENSP00000340361.3:p.Glu395Ter
|
|
ENST00000352511.4:c.1183G>T
|
ENSP00000340361.3:p.Glu395Ter
|
|
ENST00000461232.1:n.4972G>T
|
|
|
ENST00000465020.5:n.1269G>T
|
|
|
NM_001106.3:c.1183G>T
|
NP_001097.2:p.Glu395Ter
|
|
XM_005265583.2:c.1246G>T
|
XP_005265640.1:p.Glu416Ter
|
|
XM_005265583.3:c.1246G>T
|
XP_005265640.1:p.Glu416Ter
|
|
XM_017007514.1:c.1225G>T
|
XP_016863003.1:p.Glu409Ter
|
|
XM_017007515.2:c.1201G>T
|
XP_016863004.1:p.Glu401Ter
|
|
XM_017007516.1:c.1180G>T
|
XP_016863005.1:p.Glu394Ter
|
|
NM_001106.4:c.1183G>T
MANE Select
|
NP_001097.2:p.Glu395Ter
|
|