|
NM_025074.7:c.7422C>A
MANE Select
|
NP_079350.5:p.Thr2474=
|
|
ENST00000512123.4:c.7422C>A
MANE Select
|
ENSP00000422834.2:p.Thr2474=
|
|
NM_025074.6:c.7422C>A
|
NP_079350.5:p.Thr2474=
|
|
ENST00000512123.3:c.7422C>A
|
ENSP00000422834.2:p.Thr2474=
|
|
ENST00000682513.1:c.7422C>A
|
ENSP00000508201.1:p.Thr2474=
|
|
XM_006714314.1:c.7416C>A
|
XP_006714377.1:p.Thr2472=
|
|
XM_006714316.1:c.7194C>A
|
XP_006714379.1:p.Thr2398=
|
|
XM_006714316.3:c.7194C>A
|
XP_006714379.1:p.Thr2398=
|
|
XM_011532270.1:c.5121C>A
|
XP_011530572.1:p.Thr1707=
|
|
XM_011532271.1:c.2310C>A
|
XP_011530573.1:p.Thr770=
|