ENST00000289957.3:c.1242+310C>T
MANE Select
|
ENSP00000289957.2:n.1242+310C>T
|
|
ENST00000289957.2:c.1242+310C>T
|
ENSP00000289957.2:n.1242+310C>T
|
|
NM_000749.3:c.1242+310C>T
|
NP_000740.1:n.1242+310C>T
|
|
XM_011544390.1:c.855+310C>T
|
XP_011542692.1:n.855+310C>T
|
|
NM_000749.4:c.1242+310C>T
|
NP_000740.1:n.1242+310C>T
|
|
NM_001347717.1:c.1020+310C>T
|
NP_001334646.1:n.1020+310C>T
|
|
XM_011544390.2:c.855+310C>T
|
XP_011542692.1:n.855+310C>T
|
|
NM_000749.5:c.1242+310C>T
MANE Select
|
NP_000740.1:n.1242+310C>T
|
|
NM_001347717.2:c.1020+310C>T
|
NP_001334646.1:n.1020+310C>T
|
|