ENST00000711048.1:c.1009-554G>T
|
ENSP00000518557.1:n.1009-554G>T
|
|
ENST00000402731.6:c.972G>T
|
ENSP00000384835.2:p.Leu324Phe
|
|
ENST00000404276.6:c.1173G>T
MANE Select
|
ENSP00000385747.1:p.Leu391Phe
|
|
ENST00000425190.7:c.510G>T
|
ENSP00000390244.2:p.Leu170Phe
|
|
ENST00000464581.6:c.513G>T
|
ENSP00000483777.2:p.Leu171Phe
|
|
ENST00000648295.1:n.725G>T
|
|
|
ENST00000649563.1:c.510G>T
|
ENSP00000496928.1:p.Leu170Phe
|
|
ENST00000650281.1:c.1173G>T
|
ENSP00000497000.1:p.Leu391Phe
|
|
ENST00000328354.10:c.1173G>T
|
ENSP00000329178.6:p.Leu391Phe
|
|
ENST00000348295.7:c.1086G>T
|
ENSP00000329012.5:p.Leu362Phe
|
|
ENST00000382580.6:c.1302G>T
|
ENSP00000372023.2:p.Leu434Phe
|
|
ENST00000402731.5:c.1086G>T
|
ENSP00000384835.1:p.Leu362Phe
|
|
ENST00000403642.5:c.900G>T
|
ENSP00000384919.1:p.Leu300Phe
|
|
ENST00000404276.5:c.1173G>T
|
ENSP00000385747.1:p.Leu391Phe
|
|
ENST00000405598.5:c.1173G>T
|
ENSP00000386087.1:p.Leu391Phe
|
|
ENST00000416671.5:c.*663G>T
|
ENSP00000402225.1:n.*663G>T
|
|
ENST00000417588.5:c.1082G>T
|
ENSP00000412901.1:n.1082G>T
|
|
ENST00000433728.5:c.1111G>T
|
ENSP00000404400.1:n.1111G>T
|
|
ENST00000434810.5:c.404G>T
|
|
|
ENST00000448511.5:c.1063G>T
|
ENSP00000404567.1:n.1063G>T
|
|
ENST00000456369.5:c.263+4042G>T
|
|
|
NM_001005735.1:c.1302G>T
|
NP_001005735.1:p.Leu434Phe
|
|
NM_001257387.1:c.510G>T
|
NP_001244316.1:p.Leu170Phe
|
|
NM_007194.3:c.1173G>T
|
NP_009125.1:p.Leu391Phe
|
|
NM_145862.2:c.1086G>T
|
NP_665861.1:p.Leu362Phe
|
|
XM_006724114.2:c.693G>T
|
XP_006724177.1:p.Leu231Phe
|
|
XM_006724116.2:c.630G>T
|
XP_006724179.2:p.Leu210Phe
|
|
XM_011529839.1:c.1332G>T
|
XP_011528141.1:p.Leu444Phe
|
|
XM_011529840.1:c.1245G>T
|
XP_011528142.1:p.Leu415Phe
|
|
XM_011529841.1:c.1101G>T
|
XP_011528143.1:p.Leu367Phe
|
|
XM_011529842.1:c.1002G>T
|
XP_011528144.1:p.Leu334Phe
|
|
XM_011529843.1:c.972G>T
|
XP_011528145.1:p.Leu324Phe
|
|
XM_011529845.1:c.510G>T
|
XP_011528147.1:p.Leu170Phe
|
|
XR_937805.1:n.1332G>T
|
|
|
XR_937806.1:n.1240G>T
|
|
|
NM_001349956.1:c.972G>T
|
NP_001336885.1:p.Leu324Phe
|
|
NM_007194.4:c.1173G>T
MANE Select
|
NP_009125.1:p.Leu391Phe
|
|
XM_006724114.3:c.726G>T
|
XP_006724177.2:p.Leu242Phe
|
|
XM_011529839.2:c.1332G>T
|
XP_011528141.1:p.Leu444Phe
|
|
XM_011529840.3:c.1245G>T
|
XP_011528142.1:p.Leu415Phe
|
|
XM_011529842.2:c.1002G>T
|
XP_011528144.1:p.Leu334Phe
|
|
XM_011529845.2:c.510G>T
|
XP_011528147.1:p.Leu170Phe
|
|
XM_017028560.1:c.1296G>T
|
XP_016884049.1:p.Leu432Phe
|
|
XM_017028561.2:c.510G>T
|
XP_016884050.1:p.Leu170Phe
|
|
XM_024452148.1:c.1203G>T
|
XP_024307916.1:p.Leu401Phe
|
|
XM_024452149.1:c.1116G>T
|
XP_024307917.1:p.Leu372Phe
|
|
XR_937805.2:n.1343G>T
|
|
|
XR_937806.2:n.1256G>T
|
|
|
NM_001005735.2:c.1302G>T
|
NP_001005735.1:p.Leu434Phe
|
|
NM_001257387.2:c.510G>T
|
NP_001244316.1:p.Leu170Phe
|
|
NM_001349956.2:c.972G>T
|
NP_001336885.1:p.Leu324Phe
|
|