ENST00000403665.7:c.1473T>G
MANE Select
|
ENSP00000384957.2:p.Asn491Lys
|
|
ENST00000264691.4:c.169T>G
|
|
|
ENST00000264692.8:c.1311T>G
|
ENSP00000264692.5:p.Asn437Lys
|
|
ENST00000403665.6:c.1473T>G
|
ENSP00000384957.2:p.Asn491Lys
|
|
NM_000128.3:c.1473T>G , LRG_583t1:c.1473T>G
|
NP_000119.1:p.Asn491Lys
|
|
XM_005262821.2:c.1476T>G
|
XP_005262878.1:p.Asn492Lys
|
|
XM_005262822.2:c.1476T>G
|
XP_005262879.1:p.Asn492Lys
|
|
XM_005262823.2:c.1206T>G
|
XP_005262880.1:p.Asn402Lys
|
|
XM_005262824.1:c.1476T>G
|
XP_005262881.1:p.Asn492Lys
|
|
XM_006714137.1:c.1428T>G
|
XP_006714200.1:p.Asn476Lys
|
|
XR_938706.1:n.1881T>G
|
|
|
XR_938707.1:n.1881T>G
|
|
|
XM_005262821.4:c.1476T>G
|
XP_005262878.1:p.Asn492Lys
|
|
XM_005262822.4:c.1476T>G
|
XP_005262879.1:p.Asn492Lys
|
|
XM_005262823.4:c.1206T>G
|
XP_005262880.1:p.Asn402Lys
|
|
XM_006714137.3:c.1428T>G
|
XP_006714200.1:p.Asn476Lys
|
|
XR_001741172.2:n.1947T>G
|
|
|
NM_000128.4:c.1473T>G
MANE Select
|
NP_000119.1:p.Asn491Lys
|
|