ENST00000691183.1:c.*276-110G>T
|
ENSP00000509954.1:n.*276-110G>T
|
|
ENST00000378842.8:c.688-110G>T
MANE Select
|
ENSP00000368119.4:n.688-110G>T
|
|
ENST00000378842.7:c.688-110G>T
|
ENSP00000368119.3:n.688-110G>T
|
|
ENST00000450095.6:c.361-110G>T
|
ENSP00000401956.2:n.361-110G>T
|
|
ENST00000473506.6:c.*276-110G>T
|
ENSP00000432839.2:n.*276-110G>T
|
|
ENST00000473529.5:n.847-110G>T
|
|
|
ENST00000487381.5:n.1268G>T
|
|
|
ENST00000489643.6:n.658G>T
|
|
|
ENST00000554085.5:c.*432-110G>T
|
ENSP00000450419.1:n.*432-110G>T
|
|
ENST00000554550.5:c.*308-110G>T
|
ENSP00000451435.1:n.*308-110G>T
|
|
ENST00000554638.5:n.1160-110G>T
|
|
|
ENST00000555020.5:n.1039G>T
|
|
|
ENST00000555086.5:n.692-110G>T
|
|
|
ENST00000555754.1:n.33-110G>T
|
|
|
ENST00000556244.1:c.675-110G>T
|
|
|
ENST00000556278.1:c.432+196G>T
|
ENSP00000451792.1:n.432+196G>T
|
|
ENST00000557706.5:n.1250-110G>T
|
|
|
NM_000155.3:c.688-110G>T
|
NP_000146.2:n.688-110G>T
|
|
NM_001258332.1:c.361-110G>T
|
NP_001245261.1:n.361-110G>T
|
|
NM_000155.4:c.688-110G>T
MANE Select
|
NP_000146.2:n.688-110G>T
|
|
NM_001258332.2:c.361-110G>T
|
NP_001245261.1:n.361-110G>T
|
|