ENST00000248633.9:c.2416+2T>G
MANE Select
|
ENSP00000248633.4:n.2416+2T>G
|
|
ENST00000248633.8:c.2416+2T>G
|
ENSP00000248633.4:n.2416+2T>G
|
|
ENST00000428214.5:c.2245+2T>G
|
ENSP00000394413.1:n.2245+2T>G
|
|
ENST00000438045.5:c.1450+2T>G
|
ENSP00000410438.1:n.1450+2T>G
|
|
ENST00000484913.5:n.2455+2T>G
|
|
|
ENST00000496092.1:n.216T>G
|
|
|
ENST00000496420.5:n.2094T>G
|
|
|
NM_000466.2:c.2416+2T>G
|
NP_000457.1:n.2416+2T>G
|
|
NM_001282677.1:c.2245+2T>G
|
NP_001269606.1:n.2245+2T>G
|
|
NM_001282678.1:c.1792+2T>G
|
NP_001269607.1:n.1792+2T>G
|
|
XM_005250433.3:c.667+2T>G
|
XP_005250490.1:n.667+2T>G
|
|
XR_242246.3:n.2512+2T>G
|
|
|
XM_017012319.2:c.667+2T>G
|
XP_016867808.1:n.667+2T>G
|
|
XR_001744808.2:n.1443+2T>G
|
|
|
XR_242246.5:n.2463+2T>G
|
|
|
NM_000466.3:c.2416+2T>G
MANE Select
|
NP_000457.1:n.2416+2T>G
|
|
NM_001282677.2:c.2245+2T>G
|
NP_001269606.1:n.2245+2T>G
|
|
NM_001282678.2:c.1792+2T>G
|
NP_001269607.1:n.1792+2T>G
|
|