ENST00000681617.1:c.1562T>G
|
ENSP00000505544.1:p.Leu521Arg
|
|
ENST00000681780.1:c.893T>G
|
ENSP00000505780.1:p.Leu298Arg
|
|
ENST00000370132.8:c.1436T>G
MANE Select
|
ENSP00000359151.3:p.Leu479Arg
|
|
NM_001918.3:c.1436T>G
|
NP_001909.3:p.Leu479Arg
|
|
XM_005270545.2:c.893T>G
|
XP_005270602.1:p.Leu298Arg
|
|
XM_005270546.2:c.893T>G
|
XP_005270603.1:p.Leu298Arg
|
|
XM_005270545.4:c.893T>G
|
XP_005270602.1:p.Leu298Arg
|
|
XM_017000468.2:c.893T>G
|
XP_016855957.1:p.Leu298Arg
|
|
XM_017000469.2:c.893T>G
|
XP_016855958.1:p.Leu298Arg
|
|
NM_001918.4:c.1436T>G
|
NP_001909.3:p.Leu479Arg
|
|
NM_001918.5:c.1436T>G
MANE Select
|
NP_001909.4:p.Leu479Arg
|
|
NM_001399969.1:c.893T>G
|
NP_001386898.1:p.Leu298Arg
|
|
NM_001399972.1:c.893T>G
|
NP_001386901.1:p.Leu298Arg
|
|
NR_174363.1:n.1268T>G
|
|
|
NR_174364.1:n.1609T>G
|
|
|
NR_174365.1:n.1233T>G
|
|
|
NR_174366.1:n.1535T>G
|
|
|