ENST00000578493.2:n.727T>G
|
|
|
ENST00000699291.1:c.519T>G
|
ENSP00000514272.1:p.Pro173=
|
|
ENST00000699292.1:n.434T>G
|
|
|
ENST00000225275.4:c.1394T>G
MANE Select
|
ENSP00000225275.3:p.Leu465Arg
|
|
ENST00000225275.3:c.1394T>G
|
ENSP00000225275.3:p.Leu465Arg
|
|
NM_000250.1:c.1394T>G , LRG_84t1:c.1394T>G
|
NP_000241.1:p.Leu465Arg
|
|
XM_011524821.1:c.1580T>G
|
XP_011523123.1:p.Leu527Arg
|
|
XM_011524822.1:c.1109T>G
|
XP_011523124.1:p.Leu370Arg
|
|
XM_011524823.1:c.1419T>G
|
XP_011523125.1:p.Pro473=
|
|
NM_000250.2:c.1394T>G
MANE Select
|
NP_000241.1:p.Leu465Arg
|
|