|
ENST00000552391.2:n.348G>T
|
|
|
|
ENST00000683543.2:c.13648G>T
|
ENSP00000506726.1:p.Ala4550Ser
|
|
|
ENST00000685166.1:c.13657G>T
|
ENSP00000509386.1:p.Ala4553Ser
|
|
|
ENST00000685982.1:c.139-148G>T
|
ENSP00000508613.1:n.139-148G>T
|
|
|
ENST00000691986.1:c.138+259G>T
|
ENSP00000509196.1:n.138+259G>T
|
|
|
ENST00000692637.1:c.13645G>T
|
ENSP00000509666.1:p.Ala4549Ser
|
|
|
ENST00000692973.1:c.249G>T
|
ENSP00000508893.1:n.249G>T
|
|
|
ENST00000301067.12:c.13648G>T
MANE Select
|
ENSP00000301067.7:p.Ala4550Ser
|
|
|
ENST00000301067.11:c.13648G>T
|
ENSP00000301067.7:p.Ala4550Ser
|
|
|
ENST00000552391.1:n.348G>T
|
|
|
|
NM_003482.3:c.13648G>T
|
NP_003473.3:p.Ala4550Ser
|
|
|
XM_005269162.3:c.13648G>T
|
XP_005269219.1:p.Ala4550Ser
|
|
|
XM_006719614.2:c.13657G>T
|
XP_006719677.1:p.Ala4553Ser
|
|
|
XM_006719616.2:c.13645G>T
|
XP_006719679.1:p.Ala4549Ser
|
|
|
XM_011538770.1:c.13657G>T
|
XP_011537072.1:p.Ala4553Ser
|
|
|
XM_011538771.1:c.13654G>T
|
XP_011537073.1:p.Ala4552Ser
|
|
|
XM_011538772.1:c.13648G>T
|
XP_011537074.1:p.Ala4550Ser
|
|
|
XM_011538773.1:c.13645G>T
|
XP_011537075.1:p.Ala4549Ser
|
|
|
XM_011538774.1:c.13636G>T
|
XP_011537076.1:p.Ala4546Ser
|
|
|
XM_011538775.1:c.13657G>T
|
XP_011537077.1:p.Ala4553Ser
|
|
|
XM_011538776.1:c.13564G>T
|
XP_011537078.1:p.Ala4522Ser
|
|
|
XR_944740.1:n.15977G>T
|
|
|
|
XM_005269162.4:c.13648G>T
|
XP_005269219.1:p.Ala4550Ser
|
|
|
XM_006719614.4:c.13657G>T
|
XP_006719677.1:p.Ala4553Ser
|
|
|
XM_006719616.3:c.13645G>T
|
XP_006719679.1:p.Ala4549Ser
|
|
|
XM_011538770.2:c.13657G>T
|
XP_011537072.1:p.Ala4553Ser
|
|
|
XM_011538771.2:c.13654G>T
|
XP_011537073.1:p.Ala4552Ser
|
|
|
XM_011538772.2:c.13648G>T
|
XP_011537074.1:p.Ala4550Ser
|
|
|
XM_011538773.2:c.13645G>T
|
XP_011537075.1:p.Ala4549Ser
|
|
|
XM_011538774.2:c.13636G>T
|
XP_011537076.1:p.Ala4546Ser
|
|
|
XM_011538776.2:c.13564G>T
|
XP_011537078.1:p.Ala4522Ser
|
|
|
XR_001748874.1:n.14966G>T
|
|
|
|
NM_003482.4:c.13648G>T
MANE Select
|
NP_003473.3:p.Ala4550Ser
|
|
