|
ENST00000292535.12:c.4317G>A
MANE Select
|
ENSP00000292535.7:p.Pro1439=
|
|
|
ENST00000292538.9:c.1256-24525G>A
|
ENSP00000292538.4:n.1256-24525G>A
|
|
|
ENST00000437600.9:c.1250-24525G>A
|
ENSP00000414091.5:n.1250-24525G>A
|
|
|
ENST00000546411.7:c.4317G>A
|
ENSP00000450125.3:p.Pro1439=
|
|
|
ENST00000622516.6:c.1256-24525G>A
MANE Plus Clinical
|
ENSP00000484760.2:n.1256-24525G>A
|
|
|
ENST00000645010.1:c.4182G>A
|
ENSP00000496653.1:p.Pro1394=
|
|
|
ENST00000646649.1:c.3876G>A
|
ENSP00000494610.1:p.Pro1292=
|
|
|
ENST00000292535.11:c.4317G>A
|
ENSP00000292535.7:p.Pro1439=
|
|
|
ENST00000292538.8:c.1256-24525G>A
|
ENSP00000292538.4:n.1256-24525G>A
|
|
|
ENST00000360264.7:c.4350G>A
|
ENSP00000353401.3:p.Pro1450=
|
|
|
ENST00000393824.7:c.1139-24525G>A
|
ENSP00000377410.3:n.1139-24525G>A
|
|
|
ENST00000425244.6:c.1118-24525G>A
|
ENSP00000409745.2:n.1118-24525G>A
|
|
|
ENST00000437600.8:c.1256-24525G>A
|
ENSP00000414091.4:n.1256-24525G>A
|
|
|
ENST00000546411.6:c.4011G>A
|
ENSP00000450125.2:p.Pro1337=
|
|
|
ENST00000547394.6:c.1208-24525G>A
|
ENSP00000449371.2:n.1208-24525G>A
|
|
|
ENST00000549414.6:c.4251G>A
|
ENSP00000446630.2:p.Pro1417=
|
|
|
ENST00000550008.6:c.4149G>A
|
ENSP00000447373.2:p.Pro1383=
|
|
|
ENST00000556210.1:c.3843G>A
|
ENSP00000451558.1:p.Pro1281=
|
|
|
ENST00000558836.5:n.1362-24525G>A
|
|
|
|
ENST00000560541.5:n.1528-24525G>A
|
|
|
|
ENST00000622516.4:c.1250-24525G>A
|
ENSP00000484760.1:n.1250-24525G>A
|
|
|
NM_001202543.1:c.4350G>A
|
NP_001189472.1:p.Pro1450=
|
|
|
NM_001202544.2:c.1208-24525G>A
|
NP_001189473.1:n.1208-24525G>A
|
|
|
NM_001202545.2:c.1118-24525G>A
|
NP_001189474.1:n.1118-24525G>A
|
|
|
NM_001202546.2:c.1139-24525G>A
|
NP_001189475.1:n.1139-24525G>A
|
|
|
NM_001913.4:c.1256-24525G>A
|
NP_001904.2:n.1256-24525G>A
|
|
|
NM_181500.3:c.1250-24525G>A
|
NP_852477.1:n.1250-24525G>A
|
|
|
NM_181552.3:c.4317G>A
|
NP_853530.2:p.Pro1439=
|
|
|
XM_005250150.1:c.4614G>A
|
XP_005250207.1:p.Pro1538=
|
|
|
XM_005250151.1:c.4611G>A
|
XP_005250208.1:p.Pro1537=
|
|
|
XM_005250154.3:c.1523-24525G>A
|
XP_005250211.1:n.1523-24525G>A
|
|
|
XM_006715854.1:c.4551G>A
|
XP_006715917.1:p.Pro1517=
|
|
|
XM_006715855.1:c.1517-24525G>A
|
XP_006715918.1:n.1517-24525G>A
|
|
|
XM_006715856.2:c.4284G>A
|
XP_006715919.1:p.Pro1428=
|
|
|
XM_011515823.1:c.4311G>A
|
XP_011514125.1:p.Pro1437=
|
|
|
XM_011515824.1:c.4305G>A
|
XP_011514126.1:p.Pro1435=
|
|
|
XM_011515825.1:c.4044G>A
|
XP_011514127.1:p.Pro1348=
|
|
|
XM_005250150.3:c.4614G>A
|
XP_005250207.1:p.Pro1538=
|
|
|
XM_006715854.2:c.4551G>A
|
XP_006715917.1:p.Pro1517=
|
|
|
XM_011515825.2:c.4044G>A
|
XP_011514127.1:p.Pro1348=
|
|
|
XM_017011760.2:c.4278G>A
|
XP_016867249.1:p.Pro1426=
|
|
|
XM_024446668.1:c.4305G>A
|
XP_024302436.1:p.Pro1435=
|
|
|
NM_181552.4:c.4317G>A
MANE Select
|
NP_853530.2:p.Pro1439=
|
|
|
NM_001202543.2:c.4350G>A
|
NP_001189472.1:p.Pro1450=
|
|
|
NM_001202544.3:c.1208-24525G>A
|
NP_001189473.1:n.1208-24525G>A
|
|
|
NM_001202545.3:c.1118-24525G>A
|
NP_001189474.1:n.1118-24525G>A
|
|
|
NM_001202546.3:c.1139-24525G>A
|
NP_001189475.1:n.1139-24525G>A
|
|
|
NM_001913.5:c.1256-24525G>A
MANE Plus Clinical
|
NP_001904.2:n.1256-24525G>A
|
|
|
NM_181500.4:c.1250-24525G>A
|
NP_852477.1:n.1250-24525G>A
|
|
