ENST00000352511.5:c.1217C>G
MANE Select
|
ENSP00000340361.3:p.Pro406Arg
|
|
ENST00000352511.4:c.1217C>G
|
ENSP00000340361.3:p.Pro406Arg
|
|
ENST00000461232.1:n.5006C>G
|
|
|
ENST00000465020.5:n.1303C>G
|
|
|
NM_001106.3:c.1217C>G
|
NP_001097.2:p.Pro406Arg
|
|
XM_005265583.2:c.1280C>G
|
XP_005265640.1:p.Pro427Arg
|
|
XM_005265583.3:c.1280C>G
|
XP_005265640.1:p.Pro427Arg
|
|
XM_017007514.1:c.1259C>G
|
XP_016863003.1:p.Pro420Arg
|
|
XM_017007515.2:c.1235C>G
|
XP_016863004.1:p.Pro412Arg
|
|
XM_017007516.1:c.1214C>G
|
XP_016863005.1:p.Pro405Arg
|
|
NM_001106.4:c.1217C>G
MANE Select
|
NP_001097.2:p.Pro406Arg
|
|