ENST00000248633.9:c.1984G>T
MANE Select
|
ENSP00000248633.4:p.Asp662Tyr
|
|
ENST00000248633.8:c.1984G>T
|
ENSP00000248633.4:p.Asp662Tyr
|
|
ENST00000428214.5:c.1900+1429G>T
|
ENSP00000394413.1:n.1900+1429G>T
|
|
ENST00000438045.5:c.1018G>T
|
ENSP00000410438.1:p.Asp340Tyr
|
|
ENST00000484913.5:n.2023G>T
|
|
|
ENST00000496420.5:n.1660G>T
|
|
|
NM_000466.2:c.1984G>T
|
NP_000457.1:p.Asp662Tyr
|
|
NM_001282677.1:c.1900+1429G>T
|
NP_001269606.1:n.1900+1429G>T
|
|
NM_001282678.1:c.1360G>T
|
NP_001269607.1:p.Asp454Tyr
|
|
XM_005250433.3:c.235G>T
|
XP_005250490.1:p.Asp79Tyr
|
|
XR_242246.3:n.2080G>T
|
|
|
XM_017012319.2:c.235G>T
|
XP_016867808.1:p.Asp79Tyr
|
|
XR_001744808.2:n.1011G>T
|
|
|
XR_242246.5:n.2031G>T
|
|
|
NM_000466.3:c.1984G>T
MANE Select
|
NP_000457.1:p.Asp662Tyr
|
|
NM_001282677.2:c.1900+1429G>T
|
NP_001269606.1:n.1900+1429G>T
|
|
NM_001282678.2:c.1360G>T
|
NP_001269607.1:p.Asp454Tyr
|
|