ENST00000308736.7:c.1238T=
MANE Select
|
ENSP00000311135.2:p.Val413=
|
|
ENST00000544745.2:c.709T=
|
|
|
ENST00000679875.1:n.1310T=
|
|
|
ENST00000308736.6:c.1238T=
|
ENSP00000311135.2:p.Val413=
|
|
ENST00000539298.1:n.1338T=
|
|
|
ENST00000544745.1:c.599T=
|
ENSP00000439009.1:p.Val200=
|
|
NM_032656.3:c.1238T=
|
NP_116045.2:p.Val413=
|
|
XM_005253590.2:c.1238T=
|
XP_005253647.1:p.Val413=
|
|
XM_011538597.1:c.1238T=
|
XP_011536899.1:p.Val413=
|
|
XM_011538598.1:c.1238T=
|
XP_011536900.1:p.Val413=
|
|
XM_011538599.1:c.1238T=
|
XP_011536901.1:p.Val413=
|
|
XM_011538600.1:c.1238T=
|
XP_011536902.1:p.Val413=
|
|
XM_005253590.3:c.1238T=
|
XP_005253647.1:p.Val413=
|
|
XM_011538598.2:c.1238T=
|
XP_011536900.1:p.Val413=
|
|
XM_011538600.2:c.1238T=
|
XP_011536902.1:p.Val413=
|
|
XR_001748819.1:n.1341T=
|
|
|
XR_001748820.1:n.1341T=
|
|
|
NM_032656.4:c.1238T=
MANE Select
|
NP_116045.2:p.Val413=
|
|