ENST00000405460.9:c.11550A>G
MANE Select
|
ENSP00000384582.2:p.Lys3850=
|
|
ENST00000425867.3:c.681A>G
|
ENSP00000392618.3:p.Lys227=
|
|
ENST00000639431.1:c.265+78946A>G
|
ENSP00000491057.1:n.265+78946A>G
|
|
ENST00000640374.1:n.4694A>G
|
|
|
ENST00000640464.1:n.1969A>G
|
|
|
ENST00000405460.6:c.11550A>G
|
ENSP00000384582.2:p.Lys3850=
|
|
ENST00000509621.1:c.4247A>G
|
|
|
NM_032119.3:c.11550A>G
|
NP_115495.3:p.Lys3850=
|
|
NR_003149.1:n.11563A>G
|
|
|
XM_011543675.1:c.11547A>G
|
XP_011541977.1:p.Lys3849=
|
|
XM_011543676.1:c.11469A>G
|
XP_011541978.1:p.Lys3823=
|
|
XM_011543677.1:c.8853A>G
|
XP_011541979.1:p.Lys2951=
|
|
XM_011543678.1:c.11550A>G
|
XP_011541980.1:p.Lys3850=
|
|
NM_032119.4:c.11550A>G
MANE Select
|
NP_115495.3:p.Lys3850=
|
|
XM_017009963.2:c.11571A>G
|
XP_016865452.1:p.Lys3857=
|
|
XM_017009964.2:c.11568A>G
|
XP_016865453.1:p.Lys3856=
|
|
XM_017009965.1:c.11568A>G
|
XP_016865454.1:p.Lys3856=
|
|
XM_017009966.2:c.11490A>G
|
XP_016865455.1:p.Lys3830=
|
|
XM_017009967.1:c.11475A>G
|
XP_016865456.1:p.Lys3825=
|
|
XM_017009968.2:c.11571A>G
|
XP_016865457.1:p.Lys3857=
|
|
XM_017009969.2:c.11571A>G
|
XP_016865458.1:p.Lys3857=
|
|
XM_017009970.2:c.11571A>G
|
XP_016865459.1:p.Lys3857=
|
|
XM_017009971.2:c.11571A>G
|
XP_016865460.1:p.Lys3857=
|
|
XM_017009972.1:c.4689A>G
|
XP_016865461.1:p.Lys1563=
|
|
XM_017009973.1:c.4668A>G
|
XP_016865462.1:p.Lys1556=
|
|
NR_003149.2:n.11566A>G
|
|
|