ENST00000352511.5:c.1195C>A
MANE Select
|
ENSP00000340361.3:p.Arg399Ser
|
|
ENST00000352511.4:c.1195C>A
|
ENSP00000340361.3:p.Arg399Ser
|
|
ENST00000461232.1:n.4984C>A
|
|
|
ENST00000465020.5:n.1281C>A
|
|
|
NM_001106.3:c.1195C>A
|
NP_001097.2:p.Arg399Ser
|
|
XM_005265583.2:c.1258C>A
|
XP_005265640.1:p.Arg420Ser
|
|
XM_005265583.3:c.1258C>A
|
XP_005265640.1:p.Arg420Ser
|
|
XM_017007514.1:c.1237C>A
|
XP_016863003.1:p.Arg413Ser
|
|
XM_017007515.2:c.1213C>A
|
XP_016863004.1:p.Arg405Ser
|
|
XM_017007516.1:c.1192C>A
|
XP_016863005.1:p.Arg398Ser
|
|
NM_001106.4:c.1195C>A
MANE Select
|
NP_001097.2:p.Arg399Ser
|
|