|
NM_016032.4:c.674+10G>A
MANE Select
|
NP_057116.2:n.674+10G>A
|
|
ENST00000357166.11:c.674+10G>A
MANE Select
|
ENSP00000349689.6:n.674+10G>A
|
|
NM_001008222.2:c.674+10G>A
|
NP_001008223.1:n.674+10G>A
|
|
NM_001008222.3:c.674+10G>A
|
NP_001008223.1:n.674+10G>A
|
|
NM_016032.3:c.674+10G>A
|
NP_057116.2:n.674+10G>A
|
|
ENST00000357166.10:c.674+10G>A
|
ENSP00000349689.6:n.674+10G>A
|
|
ENST00000371064.7:c.674+10G>A
|
ENSP00000360103.3:n.674+10G>A
|
|
ENST00000433917.5:c.415+10G>A
|
|
|
XM_011531347.1:c.684G>A
|
XP_011529649.1:p.Pro228=
|
|
XR_001755694.2:n.1078G>A
|
|