ENST00000388922.9:c.1458G>A
MANE Select
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ENSP00000373574.4:p.Lys486=
|
|
ENST00000388922.8:c.1458G>A
|
ENSP00000373574.4:p.Lys486=
|
|
ENST00000419526.6:c.936G>A
|
ENSP00000392492.2:p.Lys312=
|
|
ENST00000550683.5:c.1500G>A
|
ENSP00000447884.1:p.Lys500=
|
|
NM_000020.2:c.1458G>A , LRG_543t1:c.1458G>A
|
NP_000011.2:p.Lys486=
|
|
NM_001077401.1:c.1458G>A
|
NP_001070869.1:p.Lys486=
|
|
XM_005269235.2:c.1458G>A
|
XP_005269292.1:p.Lys486=
|
|
XM_011539008.1:c.1188G>A
|
XP_011537310.1:p.Lys396=
|
|
XM_024449279.1:c.669G>A
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XP_024305047.1:p.Lys223=
|
|
NM_000020.3:c.1458G>A
MANE Select
|
NP_000011.2:p.Lys486=
|
|
NM_001077401.2:c.1458G>A
|
NP_001070869.1:p.Lys486=
|
|