ENST00000296051.7:c.1164T>A
MANE Select
|
ENSP00000296051.2:p.Ser388Arg
|
|
ENST00000296051.6:c.1164T>A
|
ENSP00000296051.2:p.Ser388Arg
|
|
ENST00000460120.5:c.669T>A
|
ENSP00000418230.1:p.Ser223Arg
|
|
ENST00000462030.5:n.1763T>A
|
|
|
ENST00000486530.1:n.1197T>A
|
|
|
NM_001308258.1:c.669T>A
|
NP_001295187.1:p.Ser223Arg
|
|
NM_032383.3:c.1164T>A
|
NP_115759.2:p.Ser388Arg
|
|
NM_032383.4:c.1164T>A
|
NP_115759.2:p.Ser388Arg
|
|
XM_005247834.3:c.1164T>A
|
XP_005247891.1:p.Ser388Arg
|
|
XM_006713788.1:c.1164T>A
|
XP_006713851.1:p.Ser388Arg
|
|
XR_924201.1:n.1279T>A
|
|
|
XM_005247834.4:c.1164T>A
|
XP_005247891.1:p.Ser388Arg
|
|
XM_017007323.2:c.1164T>A
|
XP_016862812.1:p.Ser388Arg
|
|
XR_001740326.2:n.1264T>A
|
|
|
XR_001740327.2:n.1264T>A
|
|
|
XR_001740328.2:n.1264T>A
|
|
|
XR_924201.3:n.1264T>A
|
|
|
NM_001308258.2:c.669T>A
|
NP_001295187.1:p.Ser223Arg
|
|
NM_032383.5:c.1164T>A
MANE Select
|
NP_115759.2:p.Ser388Arg
|
|