|
NM_003482.4:c.13402C>T
MANE Select
|
NP_003473.3:p.Arg4468Trp
|
|
ENST00000301067.12:c.13402C>T
MANE Select
|
ENSP00000301067.7:p.Arg4468Trp
|
|
NM_003482.3:c.13402C>T
|
NP_003473.3:p.Arg4468Trp
|
|
ENST00000301067.11:c.13402C>T
|
ENSP00000301067.7:p.Arg4468Trp
|
|
ENST00000552391.1:n.102C>T
|
|
|
ENST00000552391.2:n.102C>T
|
|
|
ENST00000683543.2:c.13402C>T
|
ENSP00000506726.1:p.Arg4468Trp
|
|
ENST00000685166.1:c.13411C>T
|
ENSP00000509386.1:p.Arg4471Trp
|
|
ENST00000685554.1:c.1762C>T
|
ENSP00000508640.1:p.Arg588Trp
|
|
ENST00000685982.1:c.10C>T
|
ENSP00000508613.1:p.Arg4Trp
|
|
ENST00000691986.1:c.10C>T
|
ENSP00000509196.1:p.Arg4Trp
|
|
ENST00000692637.1:c.13399C>T
|
ENSP00000509666.1:p.Arg4467Trp
|
|
ENST00000692841.1:c.4881C>T
|
ENSP00000508711.1:n.4881C>T
|
|
ENST00000692973.1:c.10C>T
|
ENSP00000508893.1:p.Arg4Trp
|
|
XM_005269162.3:c.13402C>T
|
XP_005269219.1:p.Arg4468Trp
|
|
XM_005269162.4:c.13402C>T
|
XP_005269219.1:p.Arg4468Trp
|
|
XM_006719614.2:c.13411C>T
|
XP_006719677.1:p.Arg4471Trp
|
|
XM_006719614.4:c.13411C>T
|
XP_006719677.1:p.Arg4471Trp
|
|
XM_006719616.2:c.13399C>T
|
XP_006719679.1:p.Arg4467Trp
|
|
XM_006719616.3:c.13399C>T
|
XP_006719679.1:p.Arg4467Trp
|
|
XM_011538770.1:c.13411C>T
|
XP_011537072.1:p.Arg4471Trp
|
|
XM_011538770.2:c.13411C>T
|
XP_011537072.1:p.Arg4471Trp
|
|
XM_011538771.1:c.13408C>T
|
XP_011537073.1:p.Arg4470Trp
|
|
XM_011538771.2:c.13408C>T
|
XP_011537073.1:p.Arg4470Trp
|
|
XM_011538772.1:c.13402C>T
|
XP_011537074.1:p.Arg4468Trp
|
|
XM_011538772.2:c.13402C>T
|
XP_011537074.1:p.Arg4468Trp
|
|
XM_011538773.1:c.13399C>T
|
XP_011537075.1:p.Arg4467Trp
|
|
XM_011538773.2:c.13399C>T
|
XP_011537075.1:p.Arg4467Trp
|
|
XM_011538774.1:c.13390C>T
|
XP_011537076.1:p.Arg4464Trp
|
|
XM_011538774.2:c.13390C>T
|
XP_011537076.1:p.Arg4464Trp
|
|
XM_011538775.1:c.13411C>T
|
XP_011537077.1:p.Arg4471Trp
|
|
XM_011538776.1:c.13318C>T
|
XP_011537078.1:p.Arg4440Trp
|
|
XM_011538776.2:c.13318C>T
|
XP_011537078.1:p.Arg4440Trp
|
|
XR_001748874.1:n.14720C>T
|
|
|
XR_944740.1:n.15731C>T
|
|
