ENST00000257904.11:c.582T>C
MANE Select
|
ENSP00000257904.5:p.Pro194=
|
|
ENST00000257904.10:c.582T>C
|
ENSP00000257904.5:p.Pro194=
|
|
ENST00000312990.10:c.265-35T>C
|
ENSP00000316889.6:n.265-35T>C
|
|
ENST00000546489.5:c.360T>C
|
ENSP00000447779.1:p.Pro120=
|
|
ENST00000547281.5:c.360T>C
|
ENSP00000447274.1:p.Pro120=
|
|
ENST00000549606.5:c.-157-1202T>C
|
ENSP00000447005.1:n.-157-1202T>C
|
|
ENST00000550419.5:c.523-143T>C
|
ENSP00000448098.1:n.523-143T>C
|
|
ENST00000551800.5:c.360T>C
|
ENSP00000449391.1:p.Pro120=
|
|
ENST00000551888.5:n.443-35T>C
|
|
|
ENST00000552254.5:c.582T>C
|
ENSP00000449179.1:p.Pro194=
|
|
ENST00000553237.5:c.*221T>C
|
ENSP00000448885.1:n.*221T>C
|
|
NM_000075.3:c.582T>C
|
NP_000066.1:p.Pro194=
|
|
NM_000075.4:c.582T>C
MANE Select
|
NP_000066.1:p.Pro194=
|
|