ENST00000697146.1:c.*103+29T>G
|
ENSP00000513135.1:n.*103+29T>G
|
|
ENST00000337929.8:c.507+29T>G
MANE Select
|
ENSP00000338010.3:n.507+29T>G
|
|
ENST00000337929.7:c.507+29T>G
|
ENSP00000338010.3:n.507+29T>G
|
|
ENST00000395754.4:c.507+29T>G
|
ENSP00000379103.4:n.507+29T>G
|
|
ENST00000561953.1:n.447+29T>G
|
|
|
ENST00000564089.5:c.507+29T>G
|
ENSP00000456707.1:n.507+29T>G
|
|
NM_021798.3:c.507+29T>G
|
NP_068570.1:n.507+29T>G
|
|
NM_181078.2:c.507+29T>G
|
NP_851564.1:n.507+29T>G
|
|
NM_181079.4:c.573+29T>G
|
NP_851565.4:n.573+29T>G
|
|
XM_011545857.1:c.573+29T>G
|
XP_011544159.1:n.573+29T>G
|
|
XM_011545858.1:c.136-1397T>G
|
XP_011544160.1:n.136-1397T>G
|
|
XM_011545857.3:c.573+29T>G
|
XP_011544159.1:n.573+29T>G
|
|
XM_011545858.3:c.136-1397T>G
|
XP_011544160.1:n.136-1397T>G
|
|
XM_017023257.2:c.507+29T>G
|
XP_016878746.1:n.507+29T>G
|
|
NM_181078.3:c.507+29T>G
MANE Select
|
NP_851564.1:n.507+29T>G
|
|
NM_021798.4:c.507+29T>G
|
NP_068570.1:n.507+29T>G
|
|
NM_181079.5:c.573+29T>G
|
NP_851565.4:n.573+29T>G
|
|