ENST00000402696.9:c.1846G=
MANE Select
|
ENSP00000385834.3:p.Val616=
|
|
ENST00000402696.7:c.1846G=
|
ENSP00000385834.3:p.Val616=
|
|
ENST00000461695.1:c.577G=
|
|
|
ENST00000467842.1:n.2840G=
|
|
|
NM_001063.3:c.1846G=
|
NP_001054.1:p.Val616=
|
|
XM_011513100.1:c.1846G=
|
XP_011511402.1:p.Val616=
|
|
NM_001354703.1:c.1714G=
|
NP_001341632.1:p.Val572=
|
|
NM_001354704.1:c.1465G=
|
NP_001341633.1:p.Val489=
|
|
NM_001063.4:c.1846G=
MANE Select
|
NP_001054.2:p.Val616=
|
|
NM_001354703.2:c.1714G=
|
NP_001341632.2:p.Val572=
|
|
NM_001354704.2:c.1465G=
|
NP_001341633.2:p.Val489=
|
|