ENST00000264595.7:c.394+278A>G
MANE Select
|
ENSP00000264595.2:n.394+278A>G
|
|
ENST00000264595.6:c.394+278A>G
|
ENSP00000264595.2:n.394+278A>G
|
|
ENST00000502310.5:c.49+278A>G
|
ENSP00000423798.1:n.49+278A>G
|
|
ENST00000506853.5:n.428+278A>G
|
|
|
ENST00000510635.1:c.90+278A>G
|
|
|
ENST00000510955.5:n.316-441A>G
|
|
|
NM_000027.3:c.394+278A>G
|
NP_000018.2:n.394+278A>G
|
|
NM_001171988.1:c.394+278A>G
|
NP_001165459.1:n.394+278A>G
|
|
NR_033655.1:n.522+278A>G
|
|
|
XM_006714123.2:c.394+278A>G
|
XP_006714186.1:n.394+278A>G
|
|
XR_001741155.2:n.488+278A>G
|
|
|
NM_000027.4:c.394+278A>G
MANE Select
|
NP_000018.2:n.394+278A>G
|
|
NM_001171988.2:c.394+278A>G
|
NP_001165459.1:n.394+278A>G
|
|
NR_033655.2:n.456+278A>G
|
|
|