ENST00000405460.9:c.11529A>G
MANE Select
|
ENSP00000384582.2:p.Ile3843Met
|
|
ENST00000425867.3:c.660A>G
|
ENSP00000392618.3:p.Ile220Met
|
|
ENST00000639431.1:c.265+78925A>G
|
ENSP00000491057.1:n.265+78925A>G
|
|
ENST00000640374.1:n.4673A>G
|
|
|
ENST00000640464.1:n.1948A>G
|
|
|
ENST00000405460.6:c.11529A>G
|
ENSP00000384582.2:p.Ile3843Met
|
|
ENST00000509621.1:c.4226A>G
|
|
|
NM_032119.3:c.11529A>G
|
NP_115495.3:p.Ile3843Met
|
|
NR_003149.1:n.11542A>G
|
|
|
XM_011543675.1:c.11526A>G
|
XP_011541977.1:p.Ile3842Met
|
|
XM_011543676.1:c.11448A>G
|
XP_011541978.1:p.Ile3816Met
|
|
XM_011543677.1:c.8832A>G
|
XP_011541979.1:p.Ile2944Met
|
|
XM_011543678.1:c.11529A>G
|
XP_011541980.1:p.Ile3843Met
|
|
NM_032119.4:c.11529A>G
MANE Select
|
NP_115495.3:p.Ile3843Met
|
|
XM_017009963.2:c.11550A>G
|
XP_016865452.1:p.Ile3850Met
|
|
XM_017009964.2:c.11547A>G
|
XP_016865453.1:p.Ile3849Met
|
|
XM_017009965.1:c.11547A>G
|
XP_016865454.1:p.Ile3849Met
|
|
XM_017009966.2:c.11469A>G
|
XP_016865455.1:p.Ile3823Met
|
|
XM_017009967.1:c.11454A>G
|
XP_016865456.1:p.Ile3818Met
|
|
XM_017009968.2:c.11550A>G
|
XP_016865457.1:p.Ile3850Met
|
|
XM_017009969.2:c.11550A>G
|
XP_016865458.1:p.Ile3850Met
|
|
XM_017009970.2:c.11550A>G
|
XP_016865459.1:p.Ile3850Met
|
|
XM_017009971.2:c.11550A>G
|
XP_016865460.1:p.Ile3850Met
|
|
XM_017009972.1:c.4668A>G
|
XP_016865461.1:p.Ile1556Met
|
|
XM_017009973.1:c.4647A>G
|
XP_016865462.1:p.Ile1549Met
|
|
NR_003149.2:n.11545A>G
|
|
|