ENST00000405460.9:c.10876A>C
MANE Select
|
ENSP00000384582.2:p.Lys3626Gln
|
|
ENST00000425867.3:c.7A>C
|
ENSP00000392618.3:p.Lys3Gln
|
|
ENST00000639431.1:c.265+69488A>C
|
ENSP00000491057.1:n.265+69488A>C
|
|
ENST00000640374.1:n.4020A>C
|
|
|
ENST00000640464.1:n.1295A>C
|
|
|
ENST00000405460.6:c.10876A>C
|
ENSP00000384582.2:p.Lys3626Gln
|
|
ENST00000509621.1:c.3573A>C
|
|
|
NM_032119.3:c.10876A>C
|
NP_115495.3:p.Lys3626Gln
|
|
NR_003149.1:n.10889A>C
|
|
|
XM_011543675.1:c.10873A>C
|
XP_011541977.1:p.Lys3625Gln
|
|
XM_011543676.1:c.10795A>C
|
XP_011541978.1:p.Lys3599Gln
|
|
XM_011543677.1:c.8179A>C
|
XP_011541979.1:p.Lys2727Gln
|
|
XM_011543678.1:c.10876A>C
|
XP_011541980.1:p.Lys3626Gln
|
|
NM_032119.4:c.10876A>C
MANE Select
|
NP_115495.3:p.Lys3626Gln
|
|
XM_017009963.2:c.10897A>C
|
XP_016865452.1:p.Lys3633Gln
|
|
XM_017009964.2:c.10894A>C
|
XP_016865453.1:p.Lys3632Gln
|
|
XM_017009965.1:c.10894A>C
|
XP_016865454.1:p.Lys3632Gln
|
|
XM_017009966.2:c.10816A>C
|
XP_016865455.1:p.Lys3606Gln
|
|
XM_017009967.1:c.10801A>C
|
XP_016865456.1:p.Lys3601Gln
|
|
XM_017009968.2:c.10897A>C
|
XP_016865457.1:p.Lys3633Gln
|
|
XM_017009969.2:c.10897A>C
|
XP_016865458.1:p.Lys3633Gln
|
|
XM_017009970.2:c.10897A>C
|
XP_016865459.1:p.Lys3633Gln
|
|
XM_017009971.2:c.10897A>C
|
XP_016865460.1:p.Lys3633Gln
|
|
XM_017009972.1:c.4015A>C
|
XP_016865461.1:p.Lys1339Gln
|
|
XM_017009973.1:c.3994A>C
|
XP_016865462.1:p.Lys1332Gln
|
|
NR_003149.2:n.10892A>C
|
|
|