ENST00000262027.10:c.1461G>T
MANE Select
|
ENSP00000262027.5:p.Arg487=
|
|
ENST00000262027.9:c.1461G>T
|
ENSP00000262027.5:p.Arg487=
|
|
ENST00000447721.6:n.1103G>T
|
|
|
ENST00000537638.6:c.1461G>T
|
ENSP00000446168.2:p.Arg487=
|
|
ENST00000545888.6:c.*962G>T
|
ENSP00000439307.2:n.*962G>T
|
|
ENST00000546971.5:n.205G>T
|
|
|
ENST00000548630.1:n.22G>T
|
|
|
ENST00000548944.1:c.134-4705G>T
|
ENSP00000449071.1:n.134-4705G>T
|
|
ENST00000628866.2:c.*962G>T
|
ENSP00000486738.1:n.*962G>T
|
|
NM_004990.3:c.1461G>T
|
NP_004981.2:p.Arg487=
|
|
XM_006719398.2:c.759G>T
|
XP_006719461.1:p.Arg253=
|
|
XM_011538353.1:c.1461G>T
|
XP_011536655.1:p.Arg487=
|
|
XM_006719398.4:c.759G>T
|
XP_006719461.1:p.Arg253=
|
|
XR_001748704.2:n.1484G>T
|
|
|
XR_002957327.1:n.1408G>T
|
|
|
NM_004990.4:c.1461G>T
MANE Select
|
NP_004981.2:p.Arg487=
|
|