|
NM_002911.4:c.2080C>T
MANE Select
|
NP_002902.2:p.Arg694Trp
|
|
ENST00000262803.10:c.2080C>T
MANE Select
|
ENSP00000262803.5:p.Arg694Trp
|
|
NM_001297549.1:c.2113C>T
|
NP_001284478.1:p.Arg705Trp
|
|
NM_001297549.2:c.2113C>T
|
NP_001284478.1:p.Arg705Trp
|
|
NM_002911.3:c.2080C>T
|
NP_002902.2:p.Arg694Trp
|
|
ENST00000262803.9:c.2080C>T
|
ENSP00000262803.4:p.Arg694Trp
|
|
ENST00000594504.6:n.2398C>T
|
|
|
ENST00000599848.5:c.2113C>T
|
ENSP00000470142.1:p.Arg705Trp
|
|
ENST00000601981.6:n.2003C>T
|
|
|
ENST00000704676.1:c.2065C>T
|
ENSP00000515988.1:p.Arg689Trp
|
|
ENST00000704677.1:c.*911C>T
|
ENSP00000515989.1:n.*911C>T
|
|
ENST00000704679.1:n.1670C>T
|
|
|
XM_017027105.2:c.2137C>T
|
XP_016882594.1:p.Arg713Trp
|
|
XM_017027106.2:c.2104C>T
|
XP_016882595.1:p.Arg702Trp
|