NM_001397406.1:c.308-269C>G
MANE Select
|
NP_001384335.1:n.308-269C>G
|
ENST00000393708.3:c.317-269C>G
MANE Select
|
ENSP00000377311.4:n.317-269C>G
|
NM_001031734.3:c.317-269C>G
|
NP_001026904.2:n.317-269C>G
|
NM_001031734.4:c.317-269C>G
|
NP_001026904.2:n.317-269C>G
|
ENST00000343376.8:n.417-269C>G
|
|
ENST00000452032.6:c.317-269C>G
|
ENSP00000408510.2:n.317-269C>G
|
ENST00000453681.1:n.414-269C>G
|
|
ENST00000460631.5:n.520-269C>G
|
|
ENST00000492239.5:c.-98-269C>G
|
ENSP00000488228.1:n.-98-269C>G
|
ENST00000493771.2:n.172-269C>G
|
|
ENST00000494368.5:c.-98-269C>G
|
ENSP00000467188.1:n.-98-269C>G
|
ENST00000706663.1:c.52-787C>G
|
ENSP00000516489.1:n.52-787C>G
|