ENST00000378823.8:c.1871G>C
MANE Select
|
ENSP00000368100.4:p.Ser624Thr
|
|
ENST00000638452.2:c.1574G>C
|
ENSP00000492349.2:p.Ser525Thr
|
|
ENST00000638504.1:n.1480-158G>C
|
|
|
ENST00000638568.2:c.1574G>C
|
ENSP00000491158.2:p.Ser525Thr
|
|
ENST00000639899.1:n.2390G>C
|
|
|
ENST00000640655.2:c.1574G>C
|
ENSP00000491596.2:p.Ser525Thr
|
|
ENST00000651160.1:c.*16-158G>C
|
ENSP00000498829.1:n.*16-158G>C
|
|
ENST00000651658.1:n.2414G>C
|
|
|
ENST00000651723.1:c.*1954G>C
|
ENSP00000498237.1:n.*1954G>C
|
|
ENST00000652016.1:c.*89-158G>C
|
ENSP00000498267.1:n.*89-158G>C
|
|
ENST00000652485.1:c.1904G>C
|
ENSP00000498973.1:p.Ser635Thr
|
|
ENST00000378823.7:c.1871G>C
|
ENSP00000368100.4:p.Ser624Thr
|
|
ENST00000423956.5:c.*57G>C
|
ENSP00000390971.1:n.*57G>C
|
|
ENST00000453394.5:c.1688G>C
|
ENSP00000400049.1:p.Ser563Thr
|
|
ENST00000533482.5:c.*1497G>C
|
ENSP00000431225.1:n.*1497G>C
|
|
NM_005732.3:c.1871G>C
|
NP_005723.2:p.Ser624Thr
|
|
NM_005732.4:c.1871G>C
MANE Select
|
NP_005723.2:p.Ser624Thr
|
|