ENST00000368666.7:c.1053C>T
MANE Select
|
ENSP00000357655.4:p.Leu351=
|
|
ENST00000639360.1:c.954C>T
|
ENSP00000491774.1:p.Leu318=
|
|
ENST00000230529.9:c.1053C>T
|
ENSP00000230529.5:p.Leu351=
|
|
ENST00000361714.5:c.1053C>T
|
ENSP00000354734.2:p.Leu351=
|
|
ENST00000368663.4:c.*359C>T
|
ENSP00000357652.4:n.*359C>T
|
|
ENST00000368664.7:c.*457C>T
|
ENSP00000357653.3:n.*457C>T
|
|
ENST00000368666.6:c.1107C>T
|
ENSP00000357655.3:p.Leu369=
|
|
ENST00000409166.5:c.381C>T
|
ENSP00000386467.1:p.Leu127=
|
|
ENST00000454589.5:c.*457C>T
|
ENSP00000395928.1:n.*457C>T
|
|
ENST00000604763.5:c.1053C>T
|
ENSP00000473777.1:p.Leu351=
|
|
ENST00000613648.1:n.888C>T
|
|
|
ENST00000620524.3:n.984C>T
|
|
|
NM_003880.3:c.1053C>T
|
NP_003871.1:p.Leu351=
|
|
NM_198239.1:c.1107C>T
|
NP_937882.1:p.Leu369=
|
|
NR_125353.1:n.1307C>T
|
|
|
NR_125354.1:n.1227C>T
|
|
|
XM_011536220.1:c.1053C>T
|
XP_011534522.1:p.Leu351=
|
|
XM_011536221.1:c.*457C>T
|
XP_011534523.1:n.*457C>T
|
|
XM_011536223.1:c.471C>T
|
XP_011534525.1:p.Leu157=
|
|
XM_011536223.3:c.471C>T
|
XP_011534525.1:p.Leu157=
|
|
XR_001743705.1:n.1655C>T
|
|
|
NM_003880.4:c.1053C>T
|
NP_003871.1:p.Leu351=
|
|
NM_198239.2:c.1053C>T
MANE Select
|
NP_937882.2:p.Leu351=
|
|
NR_125353.2:n.1371C>T
|
|
|
NR_125354.3:n.1198C>T
|
|
|