ENST00000296684.10:c.186T>C
MANE Select
|
ENSP00000296684.5:p.Thr62=
|
|
ENST00000296684.9:c.186T>C
|
ENSP00000296684.5:p.Thr62=
|
|
ENST00000502423.5:c.*53T>C
|
ENSP00000422177.1:n.*53T>C
|
|
ENST00000506765.1:c.174T>C
|
ENSP00000424570.1:p.Thr58=
|
|
ENST00000506974.5:c.358T>C
|
ENSP00000425967.1:p.Tyr120His
|
|
ENST00000507026.5:c.*160T>C
|
ENSP00000424993.1:n.*160T>C
|
|
ENST00000509443.1:n.47T>C
|
|
|
NM_002495.2:c.186T>C
|
NP_002486.1:p.Thr62=
|
|
XM_005248525.3:c.186T>C
|
XP_005248582.1:p.Thr62=
|
|
XM_011543415.1:c.12T>C
|
XP_011541717.1:p.Thr4=
|
|
NM_001318051.1:c.186T>C
|
NP_001304980.1:p.Thr62=
|
|
NM_002495.3:c.186T>C
|
NP_002486.1:p.Thr62=
|
|
NR_134473.1:n.388T>C
|
|
|
NR_134474.1:n.305T>C
|
|
|
NR_134475.1:n.340T>C
|
|
|
NM_002495.4:c.186T>C
MANE Select
|
NP_002486.1:p.Thr62=
|
|
NM_001318051.2:c.186T>C
|
NP_001304980.1:p.Thr62=
|
|
NR_134473.2:n.382T>C
|
|
|
NR_134474.2:n.299T>C
|
|
|
NR_134475.2:n.334T>C
|
|
|