ENST00000374580.10:c.2650_2662delinsCTGGATCGTCTTG
MANE Select
|
ENSP00000363708.4:p.Leu884=
|
|
ENST00000638587.1:c.2581_2593delinsCTGGATCGTCTTG
|
ENSP00000491062.1:n.2581_2593delinsCTGGATCGTCTTG
|
|
ENST00000374574.2:c.1587-3381_1587-3369delinsCTGGATCGTCTTG
|
ENSP00000363702.2:n.1587-3381_1587-3369delinsCTGGATCGTCTTG
|
|
ENST00000374580.8:c.2650_2662delinsCTGGATCGTCTTG
|
ENSP00000363708.4:p.Leu884=
|
|
NM_001204.6:c.2650_2662delinsCTGGATCGTCTTG , LRG_712t1:c.2650_2662delinsCTGGATCGTCTTG
|
NP_001195.2:p.Leu884=
|
|
XM_011511687.1:c.2650_2662delinsCTGGATCGTCTTG
|
XP_011509989.1:p.Leu884=
|
|
XM_011511688.1:c.1587-3381_1587-3369delinsCTGGATCGTCTTG
|
XP_011509990.1:n.1587-3381_1587-3369delinsCTGGATCGTCTTG
|
|
NM_001204.7:c.2650_2662delinsCTGGATCGTCTTG
MANE Select
|
NP_001195.2:p.Leu884=
|
|