ENST00000326828.6:c.377+77C>T
MANE Select
|
ENSP00000315602.5:n.377+77C>T
|
|
ENST00000326828.5:c.377+77C>T
|
ENSP00000315602.5:n.377+77C>T
|
|
ENST00000348639.7:c.377+77C>T
|
ENSP00000267951.4:n.377+77C>T
|
|
ENST00000559658.5:c.377+77C>T
|
ENSP00000452896.1:n.377+77C>T
|
|
NM_000743.4:c.377+77C>T
|
NP_000734.2:n.377+77C>T
|
|
NM_001166694.1:c.377+77C>T
|
NP_001160166.1:n.377+77C>T
|
|
NR_046313.1:n.878+77C>T
|
|
|
XM_006720382.1:c.176+77C>T
|
XP_006720445.1:n.176+77C>T
|
|
XM_011521173.1:c.296+77C>T
|
XP_011519475.1:n.296+77C>T
|
|
XM_006720382.3:c.176+77C>T
|
XP_006720445.1:n.176+77C>T
|
|
NM_000743.5:c.377+77C>T
MANE Select
|
NP_000734.2:n.377+77C>T
|
|
NM_001166694.2:c.377+77C>T
|
NP_001160166.1:n.377+77C>T
|
|
NR_046313.2:n.579+77C>T
|
|
|