ENST00000375750.9:c.1459G>T
(MSH5)
MANE Select
|
ENSP00000364903.3:p.Asp487Tyr
|
|
ENST00000375755.8:c.1459G>T
(MSH5)
|
ENSP00000364908.3:p.Asp487Tyr
|
|
ENST00000650702.1:n.1809G>T
(MSH5)
|
|
|
ENST00000375703.7:c.1459G>T
(MSH5)
|
ENSP00000364855.3:p.Asp487Tyr
|
|
ENST00000375740.7:c.1510G>T
(MSH5)
|
ENSP00000364892.3:p.Asp504Tyr
|
|
ENST00000375750.7:c.1459G>T
(MSH5)
|
ENSP00000364903.3:p.Asp487Tyr
|
|
ENST00000375755.7:c.1459G>T
(MSH5)
|
ENSP00000364908.3:p.Asp487Tyr
|
|
ENST00000395853.5:c.481G>T
(MSH5)
|
ENSP00000379194.1:p.Asp161Tyr
|
|
ENST00000423982.6:c.1459G>T
(MSH5)
|
ENSP00000406352.2:p.Asp487Tyr
|
|
ENST00000450148.5:c.985G>T
(MSH5)
|
ENSP00000394971.1:p.Asp329Tyr
|
|
ENST00000463144.5:c.1146G>T
(MSH5)
|
|
|
ENST00000467319.1:n.662G>T
(MSH5)
|
|
|
ENST00000468136.5:n.665G>T
(MSH5)
|
|
|
ENST00000493662.6:c.1510G>T
(MSH5-SAPCD1)
|
ENSP00000417871.2:p.Asp504Tyr
|
|
ENST00000498473.6:c.32G>T
(MSH5-SAPCD1)
|
|
|
NM_002441.4:c.1459G>T
(MSH5)
|
NP_002432.1:p.Asp487Tyr
|
|
NM_025259.5:c.1510G>T
(MSH5)
|
NP_079535.4:p.Asp504Tyr
|
|
NM_172165.3:c.1459G>T
(MSH5)
|
NP_751897.1:p.Asp487Tyr
|
|
NM_172166.3:c.1459G>T
(MSH5)
|
NP_751898.1:p.Asp487Tyr
|
|
NR_037846.1:n.1638G>T
(MSH5-SAPCD1)
|
|
|
NM_172166.4:c.1459G>T
(MSH5)
MANE Select
|
NP_751898.1:p.Asp487Tyr
|
|
NM_002441.5:c.1459G>T
(MSH5)
|
NP_002432.1:p.Asp487Tyr
|
|
NM_025259.6:c.1510G>T
(MSH5)
|
NP_079535.4:p.Asp504Tyr
|
|
NM_172165.4:c.1459G>T
(MSH5)
|
NP_751897.1:p.Asp487Tyr
|
|