ENST00000695527.1:n.15G>T
|
|
|
ENST00000695558.1:c.5703G>T
|
ENSP00000512015.1:p.Glu1901Asp
|
|
ENST00000703224.1:c.*4913G>T
|
ENSP00000515242.1:n.*4913G>T
|
|
ENST00000359568.10:c.5670G>T
MANE Select
|
ENSP00000352572.5:p.Glu1890Asp
|
|
ENST00000359568.9:c.5670G>T
|
ENSP00000352572.5:p.Glu1890Asp
|
|
ENST00000480896.5:n.5939G>T
|
|
|
NM_001315529.1:c.5316G>T
|
NP_001302458.1:p.Glu1772Asp
|
|
NM_006031.5:c.5670G>T
|
NP_006022.3:p.Glu1890Asp
|
|
XM_005261124.3:c.5703G>T
|
XP_005261181.1:p.Glu1901Asp
|
|
XM_011529593.1:c.5781G>T
|
XP_011527895.1:p.Glu1927Asp
|
|
XM_011529594.1:c.5751G>T
|
XP_011527896.1:p.Glu1917Asp
|
|
XM_005261124.5:c.5703G>T
|
XP_005261181.1:p.Glu1901Asp
|
|
XM_011529594.3:c.5751G>T
|
XP_011527896.1:p.Glu1917Asp
|
|
XM_017028362.2:c.5670G>T
|
XP_016883851.1:p.Glu1890Asp
|
|
XM_017028363.1:c.5349G>T
|
XP_016883852.1:p.Glu1783Asp
|
|
XM_024452082.1:c.4587G>T
|
XP_024307850.1:p.Glu1529Asp
|
|
XM_024452083.1:c.3483G>T
|
XP_024307851.1:p.Glu1161Asp
|
|
NM_006031.6:c.5670G>T
MANE Select
|
NP_006022.3:p.Glu1890Asp
|
|
NM_001315529.2:c.5316G>T
|
NP_001302458.1:p.Glu1772Asp
|
|