ENST00000366647.9:c.696+27C>A
MANE Select
|
ENSP00000355607.4:n.696+27C>A
|
|
ENST00000644483.1:c.*382+27C>A
|
ENSP00000496537.1:n.*382+27C>A
|
|
ENST00000366647.8:c.696+27C>A
|
ENSP00000355607.4:n.696+27C>A
|
|
ENST00000416000.1:c.666+27C>A
|
ENSP00000411640.1:n.666+27C>A
|
|
ENST00000436239.5:c.513+27C>A
|
ENSP00000402811.1:n.513+27C>A
|
|
NM_001316350.1:c.513+27C>A
|
NP_001303279.1:n.513+27C>A
|
|
NM_014236.3:c.696+27C>A
|
NP_055051.1:n.696+27C>A
|
|
XM_005273313.3:c.693+27C>A
|
XP_005273370.1:n.693+27C>A
|
|
XM_011544303.1:c.369+27C>A
|
XP_011542605.1:n.369+27C>A
|
|
XM_011544304.1:c.369+27C>A
|
XP_011542606.1:n.369+27C>A
|
|
XM_005273313.4:c.693+27C>A
|
XP_005273370.1:n.693+27C>A
|
|
XM_011544303.3:c.369+27C>A
|
XP_011542605.1:n.369+27C>A
|
|
XM_011544304.2:c.369+27C>A
|
XP_011542606.1:n.369+27C>A
|
|
NM_014236.4:c.696+27C>A
MANE Select
|
NP_055051.1:n.696+27C>A
|
|
NM_001316350.2:c.513+27C>A
|
NP_001303279.1:n.513+27C>A
|
|