ENST00000356392.9:c.963+52A>G
MANE Select
|
ENSP00000348757.3:n.963+52A>G
|
|
ENST00000356392.8:c.963+52A>G
|
ENSP00000348757.3:n.963+52A>G
|
|
ENST00000586836.5:c.390+52A>G
|
ENSP00000467429.1:n.390+52A>G
|
|
ENST00000591179.5:c.783+52A>G
|
ENSP00000466800.1:n.783+52A>G
|
|
ENST00000591345.5:c.*882+52A>G
|
ENSP00000467313.1:n.*882+52A>G
|
|
NM_001302453.1:c.801+52A>G
|
NP_001289382.1:n.801+52A>G
|
|
NM_001302454.1:c.783+52A>G
|
NP_001289383.1:n.783+52A>G
|
|
NM_145045.4:c.963+52A>G
|
NP_659482.3:n.963+52A>G
|
|
XM_017026241.1:c.904+111A>G
|
XP_016881730.1:n.904+111A>G
|
|
NM_145045.5:c.963+52A>G
MANE Select
|
NP_659482.3:n.963+52A>G
|
|
NM_001302454.2:c.783+52A>G
|
NP_001289383.1:n.783+52A>G
|
|