ENST00000248633.9:c.2214G>T
MANE Select
|
ENSP00000248633.4:p.Gln738His
|
|
ENST00000248633.8:c.2214G>T
|
ENSP00000248633.4:p.Gln738His
|
|
ENST00000428214.5:c.2043G>T
|
ENSP00000394413.1:p.Gln681His
|
|
ENST00000438045.5:c.1248G>T
|
ENSP00000410438.1:p.Gln416His
|
|
ENST00000484913.5:n.2253G>T
|
|
|
ENST00000496092.1:n.12G>T
|
|
|
ENST00000496420.5:n.1890G>T
|
|
|
NM_000466.2:c.2214G>T
|
NP_000457.1:p.Gln738His
|
|
NM_001282677.1:c.2043G>T
|
NP_001269606.1:p.Gln681His
|
|
NM_001282678.1:c.1590G>T
|
NP_001269607.1:p.Gln530His
|
|
XM_005250433.3:c.465G>T
|
XP_005250490.1:p.Gln155His
|
|
XR_242246.3:n.2310G>T
|
|
|
XM_017012319.2:c.465G>T
|
XP_016867808.1:p.Gln155His
|
|
XR_001744808.2:n.1241G>T
|
|
|
XR_242246.5:n.2261G>T
|
|
|
NM_000466.3:c.2214G>T
MANE Select
|
NP_000457.1:p.Gln738His
|
|
NM_001282677.2:c.2043G>T
|
NP_001269606.1:p.Gln681His
|
|
NM_001282678.2:c.1590G>T
|
NP_001269607.1:p.Gln530His
|
|