ENST00000248633.9:c.1903A>C
MANE Select
|
ENSP00000248633.4:p.Lys635Gln
|
|
ENST00000248633.8:c.1903A>C
|
ENSP00000248633.4:p.Lys635Gln
|
|
ENST00000422866.1:c.721A>C
|
|
|
ENST00000428214.5:c.1900+1348A>C
|
ENSP00000394413.1:n.1900+1348A>C
|
|
ENST00000438045.5:c.937A>C
|
ENSP00000410438.1:p.Lys313Gln
|
|
ENST00000484913.5:n.1942A>C
|
|
|
ENST00000496420.5:n.1579A>C
|
|
|
NM_000466.2:c.1903A>C
|
NP_000457.1:p.Lys635Gln
|
|
NM_001282677.1:c.1900+1348A>C
|
NP_001269606.1:n.1900+1348A>C
|
|
NM_001282678.1:c.1279A>C
|
NP_001269607.1:p.Lys427Gln
|
|
XM_005250433.3:c.154A>C
|
XP_005250490.1:p.Lys52Gln
|
|
XR_242246.3:n.1999A>C
|
|
|
XM_017012319.2:c.154A>C
|
XP_016867808.1:p.Lys52Gln
|
|
XR_001744808.2:n.930A>C
|
|
|
XR_242246.5:n.1950A>C
|
|
|
NM_000466.3:c.1903A>C
MANE Select
|
NP_000457.1:p.Lys635Gln
|
|
NM_001282677.2:c.1900+1348A>C
|
NP_001269606.1:n.1900+1348A>C
|
|
NM_001282678.2:c.1279A>C
|
NP_001269607.1:p.Lys427Gln
|
|