ENST00000512097.10:c.1977+12T>G
|
ENSP00000427120.4:n.1977+12T>G
|
|
ENST00000512097.9:c.1977+12T>G
|
ENSP00000427120.4:n.1977+12T>G
|
|
ENST00000631899.2:c.1181+12T>G
|
|
|
ENST00000673685.1:c.1779+12T>G
MANE Select
|
ENSP00000501239.1:n.1779+12T>G
|
|
ENST00000264773.7:c.1143+12T>G
|
ENSP00000264773.2:n.1143+12T>G
|
|
ENST00000503706.5:c.99+12T>G
|
ENSP00000421439.1:n.99+12T>G
|
|
ENST00000505491.1:c.99+12T>G
|
ENSP00000421095.1:n.99+12T>G
|
|
ENST00000507750.5:n.393+12T>G
|
|
|
ENST00000512097.7:c.1143+12T>G
|
ENSP00000427120.3:n.1143+12T>G
|
|
ENST00000610748.4:c.99+12T>G
|
ENSP00000483124.1:n.99+12T>G
|
|
ENST00000631899.1:c.1143+12T>G
|
ENSP00000487849.1:n.1143+12T>G
|
|
NM_001278204.1:c.99+12T>G
|
NP_001265133.1:n.99+12T>G
|
|
NM_021614.3:c.1143+12T>G
|
NP_067627.2:n.1143+12T>G
|
|
NM_170775.2:c.99+12T>G
|
NP_740721.1:n.99+12T>G
|
|
NR_103458.1:n.542+12T>G
|
|
|
NR_130785.1:n.1539+6560A>C
|
|
|
XM_011543387.1:c.1977+12T>G
|
XP_011541689.1:n.1977+12T>G
|
|
XM_011543388.1:c.1977+12T>G
|
XP_011541690.1:n.1977+12T>G
|
|
XM_011543389.1:c.1977+12T>G
|
XP_011541691.1:n.1977+12T>G
|
|
XM_017009457.1:c.231+12T>G
|
XP_016864946.1:n.231+12T>G
|
|
NM_001372233.1:c.1977+12T>G
|
NP_001359162.1:n.1977+12T>G
|
|
NM_021614.4:c.1779+12T>G
MANE Select
|
NP_067627.3:n.1779+12T>G
|
|
NM_170775.3:c.99+12T>G
|
NP_740721.1:n.99+12T>G
|
|
NR_103458.2:n.561+12T>G
|
|
|
NM_001278204.2:c.99+12T>G
|
NP_001265133.1:n.99+12T>G
|
|
NR_174097.1:n.1430+12T>G
|
|
|