ENST00000405460.9:c.16242A>G
MANE Select
|
ENSP00000384582.2:p.Lys5414=
|
|
ENST00000425867.3:c.5196A>G
|
ENSP00000392618.3:p.Lys1732=
|
|
ENST00000638510.1:n.3509A>G
|
|
|
ENST00000639431.1:c.265+147261A>G
|
ENSP00000491057.1:n.265+147261A>G
|
|
ENST00000640061.1:n.128+1288A>G
|
|
|
ENST00000640407.1:c.2652A>G
|
ENSP00000491425.1:p.Lys884=
|
|
ENST00000405460.6:c.16242A>G
|
ENSP00000384582.2:p.Lys5414=
|
|
ENST00000425867.2:c.3225A>G
|
ENSP00000392618.2:p.Lys1075=
|
|
NM_032119.3:c.16242A>G
|
NP_115495.3:p.Lys5414=
|
|
NR_003149.1:n.16255A>G
|
|
|
XM_011543675.1:c.16239A>G
|
XP_011541977.1:p.Lys5413=
|
|
XM_011543676.1:c.16161A>G
|
XP_011541978.1:p.Lys5387=
|
|
XM_011543677.1:c.13545A>G
|
XP_011541979.1:p.Lys4515=
|
|
NM_032119.4:c.16242A>G
MANE Select
|
NP_115495.3:p.Lys5414=
|
|
XM_017009963.2:c.16263A>G
|
XP_016865452.1:p.Lys5421=
|
|
XM_017009964.2:c.16260A>G
|
XP_016865453.1:p.Lys5420=
|
|
XM_017009965.1:c.16260A>G
|
XP_016865454.1:p.Lys5420=
|
|
XM_017009966.2:c.16182A>G
|
XP_016865455.1:p.Lys5394=
|
|
XM_017009967.1:c.16167A>G
|
XP_016865456.1:p.Lys5389=
|
|
XM_017009968.2:c.16083A>G
|
XP_016865457.1:p.Lys5361=
|
|
XM_017009969.2:c.16263A>G
|
XP_016865458.1:p.Lys5421=
|
|
XM_017009972.1:c.9381A>G
|
XP_016865461.1:p.Lys3127=
|
|
XM_017009973.1:c.9360A>G
|
XP_016865462.1:p.Lys3120=
|
|
NR_003149.2:n.16258A>G
|
|
|