|
NM_003482.4:c.15286C>T
MANE Select
|
NP_003473.3:p.Gln5096Ter
|
|
ENST00000301067.12:c.15286C>T
MANE Select
|
ENSP00000301067.7:p.Gln5096Ter
|
|
NM_003482.3:c.15286C>T
|
NP_003473.3:p.Gln5096Ter
|
|
ENST00000301067.11:c.15286C>T
|
ENSP00000301067.7:p.Gln5096Ter
|
|
ENST00000683543.2:c.15286C>T
|
ENSP00000506726.1:p.Gln5096Ter
|
|
ENST00000685024.1:c.411C>T
|
|
|
ENST00000685166.1:c.15295C>T
|
ENSP00000509386.1:p.Gln5099Ter
|
|
ENST00000688411.1:c.261+1123C>T
|
ENSP00000510146.1:n.261+1123C>T
|
|
ENST00000691463.1:c.672C>T
|
ENSP00000510624.1:n.672C>T
|
|
ENST00000692637.1:c.15283C>T
|
ENSP00000509666.1:p.Gln5095Ter
|
|
XM_005269162.3:c.15286C>T
|
XP_005269219.1:p.Gln5096Ter
|
|
XM_005269162.4:c.15286C>T
|
XP_005269219.1:p.Gln5096Ter
|
|
XM_006719614.2:c.15295C>T
|
XP_006719677.1:p.Gln5099Ter
|
|
XM_006719614.4:c.15295C>T
|
XP_006719677.1:p.Gln5099Ter
|
|
XM_006719616.2:c.15283C>T
|
XP_006719679.1:p.Gln5095Ter
|
|
XM_006719616.3:c.15283C>T
|
XP_006719679.1:p.Gln5095Ter
|
|
XM_011538770.1:c.15295C>T
|
XP_011537072.1:p.Gln5099Ter
|
|
XM_011538770.2:c.15295C>T
|
XP_011537072.1:p.Gln5099Ter
|
|
XM_011538771.1:c.15292C>T
|
XP_011537073.1:p.Gln5098Ter
|
|
XM_011538771.2:c.15292C>T
|
XP_011537073.1:p.Gln5098Ter
|
|
XM_011538772.1:c.15286C>T
|
XP_011537074.1:p.Gln5096Ter
|
|
XM_011538772.2:c.15286C>T
|
XP_011537074.1:p.Gln5096Ter
|
|
XM_011538773.1:c.15283C>T
|
XP_011537075.1:p.Gln5095Ter
|
|
XM_011538773.2:c.15283C>T
|
XP_011537075.1:p.Gln5095Ter
|
|
XM_011538774.1:c.15274C>T
|
XP_011537076.1:p.Gln5092Ter
|
|
XM_011538774.2:c.15274C>T
|
XP_011537076.1:p.Gln5092Ter
|
|
XM_011538775.1:c.15229C>T
|
XP_011537077.1:p.Gln5077Ter
|
|
XM_011538776.1:c.15202C>T
|
XP_011537078.1:p.Gln5068Ter
|
|
XM_011538776.2:c.15202C>T
|
XP_011537078.1:p.Gln5068Ter
|
|
XR_001748874.1:n.15961+1123C>T
|
|
|
XR_944740.1:n.16972+1123C>T
|
|
