ENST00000706645.1:n.1553G>T
|
|
|
ENST00000281243.10:c.506G>T
MANE Select
|
ENSP00000281243.5:p.Ser169Ile
|
|
ENST00000281243.9:c.506G>T
|
ENSP00000281243.5:p.Ser169Ile
|
|
ENST00000428702.6:c.413G>T
|
ENSP00000390944.2:p.Ser138Ile
|
|
ENST00000501943.6:n.243G>T
|
|
|
ENST00000505710.1:c.364-1526G>T
|
|
|
ENST00000507439.5:c.437-1526G>T
|
ENSP00000423227.1:n.437-1526G>T
|
|
ENST00000508623.5:c.437-5035G>T
|
ENSP00000426377.1:n.437-5035G>T
|
|
ENST00000511609.1:n.238G>T
|
|
|
ENST00000513615.5:c.437-1526G>T
|
ENSP00000422759.1:n.437-1526G>T
|
|
ENST00000514300.1:c.*368-1526G>T
|
ENSP00000426039.1:n.*368-1526G>T
|
|
NM_000320.2:c.506G>T
|
NP_000311.2:p.Ser169Ile
|
|
NM_001306140.1:c.413G>T
|
NP_001293069.1:p.Ser138Ile
|
|
XR_241677.1:n.600-1526G>T
|
|
|
NR_156494.1:n.617-1526G>T
|
|
|
NM_000320.3:c.506G>T
MANE Select
|
NP_000311.2:p.Ser169Ile
|
|
NM_001306140.2:c.413G>T
|
NP_001293069.1:p.Ser138Ile
|
|
NR_156494.2:n.473-1526G>T
|
|
|