ENST00000261304.7:c.936T>A
MANE Select
|
ENSP00000261304.2:p.Ser312Arg
|
|
ENST00000261304.6:c.936T>A
|
ENSP00000261304.2:p.Ser312Arg
|
|
ENST00000393568.8:c.867T>A
|
ENSP00000377198.4:p.Ser289Arg
|
|
ENST00000393569.6:c.858T>A
|
ENSP00000377199.2:p.Ser286Arg
|
|
ENST00000474294.6:n.926T>A
|
|
|
ENST00000544807.6:c.768T>A
|
ENSP00000437513.2:p.Ser256Arg
|
|
ENST00000555000.5:c.303T>A
|
ENSP00000450472.1:p.Ser101Arg
|
|
ENST00000557316.5:c.*334T>A
|
ENSP00000452314.1:n.*334T>A
|
|
ENST00000557520.1:n.22T>A
|
|
|
ENST00000622264.4:c.926T>A
|
|
|
NM_000153.3:c.936T>A
|
NP_000144.2:p.Ser312Arg
|
|
NM_001201401.1:c.867T>A
|
NP_001188330.1:p.Ser289Arg
|
|
NM_001201402.1:c.858T>A
|
NP_001188331.1:p.Ser286Arg
|
|
XM_011536618.1:c.768T>A
|
XP_011534920.1:p.Ser256Arg
|
|
XM_011536618.2:c.768T>A
|
XP_011534920.1:p.Ser256Arg
|
|
NM_000153.4:c.936T>A
MANE Select
|
NP_000144.2:p.Ser312Arg
|
|
NM_001201401.2:c.867T>A
|
NP_001188330.1:p.Ser289Arg
|
|
NM_001201402.2:c.858T>A
|
NP_001188331.1:p.Ser286Arg
|
|