ENST00000405460.9:c.11526A>G
MANE Select
|
ENSP00000384582.2:p.Ile3842Met
|
|
ENST00000425867.3:c.657A>G
|
ENSP00000392618.3:p.Ile219Met
|
|
ENST00000639431.1:c.265+78922A>G
|
ENSP00000491057.1:n.265+78922A>G
|
|
ENST00000640374.1:n.4670A>G
|
|
|
ENST00000640464.1:n.1945A>G
|
|
|
ENST00000405460.6:c.11526A>G
|
ENSP00000384582.2:p.Ile3842Met
|
|
ENST00000509621.1:c.4223A>G
|
|
|
NM_032119.3:c.11526A>G
|
NP_115495.3:p.Ile3842Met
|
|
NR_003149.1:n.11539A>G
|
|
|
XM_011543675.1:c.11523A>G
|
XP_011541977.1:p.Ile3841Met
|
|
XM_011543676.1:c.11445A>G
|
XP_011541978.1:p.Ile3815Met
|
|
XM_011543677.1:c.8829A>G
|
XP_011541979.1:p.Ile2943Met
|
|
XM_011543678.1:c.11526A>G
|
XP_011541980.1:p.Ile3842Met
|
|
NM_032119.4:c.11526A>G
MANE Select
|
NP_115495.3:p.Ile3842Met
|
|
XM_017009963.2:c.11547A>G
|
XP_016865452.1:p.Ile3849Met
|
|
XM_017009964.2:c.11544A>G
|
XP_016865453.1:p.Ile3848Met
|
|
XM_017009965.1:c.11544A>G
|
XP_016865454.1:p.Ile3848Met
|
|
XM_017009966.2:c.11466A>G
|
XP_016865455.1:p.Ile3822Met
|
|
XM_017009967.1:c.11451A>G
|
XP_016865456.1:p.Ile3817Met
|
|
XM_017009968.2:c.11547A>G
|
XP_016865457.1:p.Ile3849Met
|
|
XM_017009969.2:c.11547A>G
|
XP_016865458.1:p.Ile3849Met
|
|
XM_017009970.2:c.11547A>G
|
XP_016865459.1:p.Ile3849Met
|
|
XM_017009971.2:c.11547A>G
|
XP_016865460.1:p.Ile3849Met
|
|
XM_017009972.1:c.4665A>G
|
XP_016865461.1:p.Ile1555Met
|
|
XM_017009973.1:c.4644A>G
|
XP_016865462.1:p.Ile1548Met
|
|
NR_003149.2:n.11542A>G
|
|
|