ENST00000405460.9:c.14021A>T
MANE Select
|
ENSP00000384582.2:p.Lys4674Met
|
|
ENST00000425867.3:c.2975A>T
|
ENSP00000392618.3:p.Lys992Met
|
|
ENST00000638510.1:n.1288A>T
|
|
|
ENST00000638975.1:c.650A>T
|
ENSP00000492630.1:p.Lys217Met
|
|
ENST00000639431.1:c.265+113620A>T
|
ENSP00000491057.1:n.265+113620A>T
|
|
ENST00000640407.1:c.431A>T
|
ENSP00000491425.1:p.Lys144Met
|
|
ENST00000405460.6:c.14021A>T
|
ENSP00000384582.2:p.Lys4674Met
|
|
ENST00000425867.2:c.1004A>T
|
ENSP00000392618.2:p.Lys335Met
|
|
NM_032119.3:c.14021A>T
|
NP_115495.3:p.Lys4674Met
|
|
NR_003149.1:n.14034A>T
|
|
|
XM_011543675.1:c.14018A>T
|
XP_011541977.1:p.Lys4673Met
|
|
XM_011543676.1:c.13940A>T
|
XP_011541978.1:p.Lys4647Met
|
|
XM_011543677.1:c.11324A>T
|
XP_011541979.1:p.Lys3775Met
|
|
XM_011543678.1:c.14021A>T
|
XP_011541980.1:p.Lys4674Met
|
|
NM_032119.4:c.14021A>T
MANE Select
|
NP_115495.3:p.Lys4674Met
|
|
XM_017009963.2:c.14042A>T
|
XP_016865452.1:p.Lys4681Met
|
|
XM_017009964.2:c.14039A>T
|
XP_016865453.1:p.Lys4680Met
|
|
XM_017009965.1:c.14039A>T
|
XP_016865454.1:p.Lys4680Met
|
|
XM_017009966.2:c.13961A>T
|
XP_016865455.1:p.Lys4654Met
|
|
XM_017009967.1:c.13946A>T
|
XP_016865456.1:p.Lys4649Met
|
|
XM_017009968.2:c.14042A>T
|
XP_016865457.1:p.Lys4681Met
|
|
XM_017009969.2:c.14042A>T
|
XP_016865458.1:p.Lys4681Met
|
|
XM_017009970.2:c.14042A>T
|
XP_016865459.1:p.Lys4681Met
|
|
XM_017009971.2:c.14042A>T
|
XP_016865460.1:p.Lys4681Met
|
|
XM_017009972.1:c.7160A>T
|
XP_016865461.1:p.Lys2387Met
|
|
XM_017009973.1:c.7139A>T
|
XP_016865462.1:p.Lys2380Met
|
|
NR_003149.2:n.14037A>T
|
|
|