ENST00000262133.11:c.2527-5C>G
MANE Select
|
ENSP00000262133.6:n.2527-5C>G
|
|
ENST00000680543.1:n.4318-5C>G
|
|
|
ENST00000262133.10:c.2527-5C>G
|
ENSP00000262133.6:n.2527-5C>G
|
|
ENST00000379935.8:n.2226-5C>G
|
|
|
ENST00000544545.2:c.1657-5C>G
|
ENSP00000444685.2:n.1657-5C>G
|
|
NM_005611.3:c.2527-5C>G
|
NP_005602.3:n.2527-5C>G
|
|
XM_005256083.3:c.2305-5C>G
|
XP_005256140.1:n.2305-5C>G
|
|
XM_011523252.1:c.2527-5C>G
|
XP_011521554.1:n.2527-5C>G
|
|
XM_011523253.1:c.1879-5C>G
|
XP_011521555.1:n.1879-5C>G
|
|
NM_001323608.1:c.2527-5C>G
|
NP_001310537.1:n.2527-5C>G
|
|
NM_001323609.1:c.2527-5C>G
|
NP_001310538.1:n.2527-5C>G
|
|
NM_001323610.1:c.2380-5C>G
|
NP_001310539.1:n.2380-5C>G
|
|
NM_001323611.1:c.2305-5C>G
|
NP_001310540.1:n.2305-5C>G
|
|
XM_011523253.2:c.1879-5C>G
|
XP_011521555.1:n.1879-5C>G
|
|
XM_017023513.1:c.1879-5C>G
|
XP_016879002.1:n.1879-5C>G
|
|
NM_005611.4:c.2527-5C>G
MANE Select
|
NP_005602.3:n.2527-5C>G
|
|
NM_001323608.2:c.2527-5C>G
|
NP_001310537.1:n.2527-5C>G
|
|
NM_001323609.2:c.2527-5C>G
|
NP_001310538.1:n.2527-5C>G
|
|
NM_001323610.2:c.2380-5C>G
|
NP_001310539.1:n.2380-5C>G
|
|