ENST00000348729.8:c.925+40A>G
MANE Select
|
ENSP00000302701.4:n.925+40A>G
|
|
ENST00000348729.7:c.925+40A>G
|
ENSP00000302701.4:n.925+40A>G
|
|
ENST00000353963.7:c.937+40A>G
|
ENSP00000302851.5:n.937+40A>G
|
|
ENST00000504513.1:c.165-284A>G
|
|
|
ENST00000506512.1:n.536+40A>G
|
|
|
NM_005847.4:c.925+40A>G
|
NP_005838.3:n.925+40A>G
|
|
NM_152685.3:c.937+40A>G
|
NP_689898.2:n.937+40A>G
|
|
XM_005272148.3:c.1045+40A>G
|
XP_005272205.3:n.1045+40A>G
|
|
XM_005272149.3:c.1033+40A>G
|
XP_005272206.3:n.1033+40A>G
|
|
XM_006714741.2:c.1045+40A>G
|
XP_006714804.2:n.1045+40A>G
|
|
XM_011543765.1:c.1045+40A>G
|
XP_011542067.1:n.1045+40A>G
|
|
XM_011543766.1:c.826+40A>G
|
XP_011542068.1:n.826+40A>G
|
|
XM_011543767.1:c.730+40A>G
|
XP_011542069.1:n.730+40A>G
|
|
XM_011543768.1:c.610+40A>G
|
XP_011542070.1:n.610+40A>G
|
|
XM_011543769.1:c.220+40A>G
|
XP_011542071.1:n.220+40A>G
|
|
XM_005272149.4:c.1033+40A>G
|
XP_005272206.3:n.1033+40A>G
|
|
XM_011543765.2:c.1045+40A>G
|
XP_011542067.1:n.1045+40A>G
|
|
NM_005847.5:c.925+40A>G
MANE Select
|
NP_005838.3:n.925+40A>G
|
|
NM_152685.4:c.937+40A>G
|
NP_689898.2:n.937+40A>G
|
|