ENST00000523731.6:c.446+145T>G
MANE Select
|
ENSP00000430338.1:n.446+145T>G
|
|
ENST00000343161.8:c.446+145T>G
|
ENSP00000343274.4:n.446+145T>G
|
|
ENST00000519053.5:c.119+145T>G
|
ENSP00000429056.1:n.119+145T>G
|
|
ENST00000519457.5:c.306-174T>G
|
ENSP00000428260.1:n.306-174T>G
|
|
ENST00000521860.5:c.408+145T>G
|
|
|
ENST00000522171.5:c.323+145T>G
|
ENSP00000429340.1:n.323+145T>G
|
|
ENST00000523206.5:c.446+145T>G
|
ENSP00000429452.1:n.446+145T>G
|
|
ENST00000523321.5:n.571+145T>G
|
|
|
ENST00000523731.5:c.446+145T>G
|
ENSP00000430338.1:n.446+145T>G
|
|
ENST00000524333.5:c.446+145T>G
|
ENSP00000427840.1:n.446+145T>G
|
|
NM_017864.3:c.446+145T>G
|
NP_060334.2:n.446+145T>G
|
|
NR_073444.1:n.588+145T>G
|
|
|
NR_073445.1:n.588+145T>G
|
|
|
XM_006716602.2:c.446+145T>G
|
XP_006716665.1:n.446+145T>G
|
|
XM_006716603.2:c.119+145T>G
|
XP_006716666.1:n.119+145T>G
|
|
XM_011517155.1:c.323+145T>G
|
XP_011515457.1:n.323+145T>G
|
|
XM_011517156.1:c.446+145T>G
|
XP_011515458.1:n.446+145T>G
|
|
XM_011517157.1:c.119+145T>G
|
XP_011515459.1:n.119+145T>G
|
|
XM_017013616.1:c.446+145T>G
|
XP_016869105.1:n.446+145T>G
|
|
XM_017013617.1:c.446+145T>G
|
XP_016869106.1:n.446+145T>G
|
|
XM_017013618.1:c.119+145T>G
|
XP_016869107.1:n.119+145T>G
|
|
XM_017013619.1:c.-838+145T>G
|
XP_016869108.1:n.-838+145T>G
|
|
NM_017864.4:c.446+145T>G
MANE Select
|
NP_060334.2:n.446+145T>G
|
|
NR_073444.2:n.591+145T>G
|
|
|
NR_073445.2:n.591+145T>G
|
|
|