|
NM_032444.4:c.1404C>T
MANE Select
|
NP_115820.2:p.Pro468=
|
|
ENST00000294008.4:c.1404C>T
MANE Select
|
ENSP00000294008.3:p.Pro468=
|
|
NM_032444.2:c.1404C>T , LRG_503t1:c.1404C>T
|
NP_115820.2:p.Pro468=
|
|
NM_032444.3:c.1404C>T
|
NP_115820.2:p.Pro468=
|
|
ENST00000294008.3:c.1404C>T
|
ENSP00000294008.3:p.Pro468=
|
|
ENST00000466154.5:n.2625C>T
|
|
|
XM_011522715.1:c.1404C>T
|
XP_011521017.1:p.Pro468=
|
|
XM_011522715.3:c.1404C>T
|
XP_011521017.1:p.Pro468=
|
|
XM_017023775.2:c.582C>T
|
XP_016879264.1:p.Pro194=
|
|
XM_024450471.1:c.1404C>T
|
XP_024306239.1:p.Pro468=
|