ENST00000248633.9:c.2397G>C
MANE Select
|
ENSP00000248633.4:p.Gln799His
|
|
ENST00000248633.8:c.2397G>C
|
ENSP00000248633.4:p.Gln799His
|
|
ENST00000428214.5:c.2226G>C
|
ENSP00000394413.1:p.Gln742His
|
|
ENST00000438045.5:c.1431G>C
|
ENSP00000410438.1:p.Gln477His
|
|
ENST00000484913.5:n.2436G>C
|
|
|
ENST00000496092.1:n.195G>C
|
|
|
ENST00000496420.5:n.2073G>C
|
|
|
NM_000466.2:c.2397G>C
|
NP_000457.1:p.Gln799His
|
|
NM_001282677.1:c.2226G>C
|
NP_001269606.1:p.Gln742His
|
|
NM_001282678.1:c.1773G>C
|
NP_001269607.1:p.Gln591His
|
|
XM_005250433.3:c.648G>C
|
XP_005250490.1:p.Gln216His
|
|
XR_242246.3:n.2493G>C
|
|
|
XM_017012319.2:c.648G>C
|
XP_016867808.1:p.Gln216His
|
|
XR_001744808.2:n.1424G>C
|
|
|
XR_242246.5:n.2444G>C
|
|
|
NM_000466.3:c.2397G>C
MANE Select
|
NP_000457.1:p.Gln799His
|
|
NM_001282677.2:c.2226G>C
|
NP_001269606.1:p.Gln742His
|
|
NM_001282678.2:c.1773G>C
|
NP_001269607.1:p.Gln591His
|
|