ENST00000334661.5:c.1246C>T
MANE Select
|
ENSP00000335600.4:p.Arg416Ter
|
|
ENST00000334661.4:c.1246C>T
|
ENSP00000335600.4:p.Arg416Ter
|
|
ENST00000461445.5:n.1343C>T
|
|
|
ENST00000463876.5:c.1309C>T
|
ENSP00000430344.1:p.Arg437Ter
|
|
ENST00000484829.5:n.393C>T
|
|
|
NM_001130964.1:c.1309C>T
|
NP_001124436.1:p.Arg437Ter
|
|
NM_006225.3:c.1246C>T
|
NP_006216.2:p.Arg416Ter
|
|
NR_024071.1:n.1740C>T
|
|
|
XM_017006622.1:c.1072C>T
|
XP_016862111.1:p.Arg358Ter
|
|
XR_001740173.2:n.1452C>T
|
|
|
NM_001130964.2:c.1309C>T
|
NP_001124436.1:p.Arg437Ter
|
|
NM_006225.4:c.1246C>T
MANE Select
|
NP_006216.2:p.Arg416Ter
|
|
NR_024071.2:n.1473C>T
|
|
|