|
NM_003482.4:c.16018C>T
MANE Select
|
NP_003473.3:p.Arg5340Ter
|
|
ENST00000301067.12:c.16018C>T
MANE Select
|
ENSP00000301067.7:p.Arg5340Ter
|
|
NM_003482.3:c.16018C>T
|
NP_003473.3:p.Arg5340Ter
|
|
ENST00000301067.11:c.16018C>T
|
ENSP00000301067.7:p.Arg5340Ter
|
|
ENST00000526209.1:c.13C>T
|
ENSP00000435714.1:p.Arg5Ter
|
|
ENST00000681974.1:n.690C>T
|
|
|
ENST00000683543.2:c.16018C>T
|
ENSP00000506726.1:p.Arg5340Ter
|
|
ENST00000683863.1:n.1733C>T
|
|
|
ENST00000684428.1:c.553C>T
|
ENSP00000507433.1:p.Arg185Ter
|
|
ENST00000684755.1:n.553C>T
|
|
|
ENST00000685024.1:c.1172C>T
|
|
|
ENST00000685166.1:c.16027C>T
|
ENSP00000509386.1:p.Arg5343Ter
|
|
ENST00000688411.1:c.495C>T
|
ENSP00000510146.1:n.495C>T
|
|
ENST00000691932.1:c.97C>T
|
ENSP00000509037.1:p.Arg33Ter
|
|
ENST00000692637.1:c.16015C>T
|
ENSP00000509666.1:p.Arg5339Ter
|
|
XM_005269162.3:c.16018C>T
|
XP_005269219.1:p.Arg5340Ter
|
|
XM_005269162.4:c.16018C>T
|
XP_005269219.1:p.Arg5340Ter
|
|
XM_006719614.2:c.16027C>T
|
XP_006719677.1:p.Arg5343Ter
|
|
XM_006719614.4:c.16027C>T
|
XP_006719677.1:p.Arg5343Ter
|
|
XM_006719616.2:c.16015C>T
|
XP_006719679.1:p.Arg5339Ter
|
|
XM_006719616.3:c.16015C>T
|
XP_006719679.1:p.Arg5339Ter
|
|
XM_011538770.1:c.16027C>T
|
XP_011537072.1:p.Arg5343Ter
|
|
XM_011538770.2:c.16027C>T
|
XP_011537072.1:p.Arg5343Ter
|
|
XM_011538771.1:c.16024C>T
|
XP_011537073.1:p.Arg5342Ter
|
|
XM_011538771.2:c.16024C>T
|
XP_011537073.1:p.Arg5342Ter
|
|
XM_011538772.1:c.16018C>T
|
XP_011537074.1:p.Arg5340Ter
|
|
XM_011538772.2:c.16018C>T
|
XP_011537074.1:p.Arg5340Ter
|
|
XM_011538773.1:c.16015C>T
|
XP_011537075.1:p.Arg5339Ter
|
|
XM_011538773.2:c.16015C>T
|
XP_011537075.1:p.Arg5339Ter
|
|
XM_011538774.1:c.16006C>T
|
XP_011537076.1:p.Arg5336Ter
|
|
XM_011538774.2:c.16006C>T
|
XP_011537076.1:p.Arg5336Ter
|
|
XM_011538775.1:c.15961C>T
|
XP_011537077.1:p.Arg5321Ter
|
|
XM_011538776.1:c.15934C>T
|
XP_011537078.1:p.Arg5312Ter
|
|
XM_011538776.2:c.15934C>T
|
XP_011537078.1:p.Arg5312Ter
|
|
XR_001748874.1:n.16195C>T
|
|
