|
NM_178554.6:c.1525C>T
(KY)
MANE Select
|
NP_848649.3:p.Arg509Trp
|
|
ENST00000423778.7:c.1525C>T
(KY)
MANE Select
|
ENSP00000397598.2:p.Arg509Trp
|
|
NM_001350859.1:c.1477C>T
(KY)
|
NP_001337788.1:p.Arg493Trp
|
|
NM_001350859.2:c.1477C>T
(KY)
|
NP_001337788.1:p.Arg493Trp
|
|
NM_001366276.1:c.1462C>T
(KY)
|
NP_001353205.1:p.Arg488Trp
|
|
NM_178554.4:c.1525C>T
(KY)
|
NP_848649.3:p.Arg509Trp
|
|
NM_178554.5:c.1525C>T
(KY)
|
NP_848649.3:p.Arg509Trp
|
|
ENST00000423778.6:c.1525C>T
(KY)
|
ENSP00000397598.2:p.Arg509Trp
|
|
ENST00000467708.2:n.106+6056G>A
(EPHB1)
|
|
|
ENST00000472904.5:n.161+6056G>A
(EPHB1)
|
|
|
ENST00000503669.1:c.*407C>T
(KY)
|
ENSP00000426777.1:n.*407C>T
|
|
ENST00000508956.5:c.1462C>T
(KY)
|
ENSP00000421297.1:p.Arg488Trp
|
|
XM_005247417.2:c.1648C>T
(KY)
|
XP_005247474.1:p.Arg550Trp
|
|
XM_005247418.2:c.1639C>T
(KY)
|
XP_005247475.1:p.Arg547Trp
|
|
XM_006713612.2:c.1585C>T
(KY)
|
XP_006713675.1:p.Arg529Trp
|
|
XM_006713612.3:c.1585C>T
(KY)
|
XP_006713675.1:p.Arg529Trp
|
|
XM_011512747.1:c.1225C>T
(KY)
|
XP_011511049.1:p.Arg409Trp
|
|
XM_017006287.1:c.1717C>T
(KY)
|
XP_016861776.1:p.Arg573Trp
|
|
XM_017006288.1:c.1663C>T
(KY)
|
XP_016861777.1:p.Arg555Trp
|
|
XM_017006290.1:c.1600C>T
(KY)
|
XP_016861779.1:p.Arg534Trp
|
|
XM_024453389.1:c.-408+6056G>A
(EPHB1)
|
XP_024309157.1:n.-408+6056G>A
|
|
XM_024453390.1:c.-408+2840G>A
(EPHB1)
|
XP_024309158.1:n.-408+2840G>A
|
|
XR_002959586.1:n.1672+6056G>A
(CEP63)
|
|
|
XR_002959589.1:n.1567+6056G>A
(CEP63)
|
|
|
XR_241572.2:n.284+6056G>A
|
|
|
XR_427411.2:n.284+6056G>A
|
|
|
XR_924521.1:n.284+6056G>A
|
|
