ENST00000691183.1:c.*341C>A
|
ENSP00000509954.1:n.*341C>A
|
|
ENST00000378842.8:c.753C>A
MANE Select
|
ENSP00000368119.4:p.Tyr251Ter
|
|
ENST00000378842.7:c.753C>A
|
ENSP00000368119.3:p.Tyr251Ter
|
|
ENST00000450095.6:c.426C>A
|
ENSP00000401956.2:p.Tyr142Ter
|
|
ENST00000473506.6:c.*341C>A
|
ENSP00000432839.2:n.*341C>A
|
|
ENST00000473529.5:n.912C>A
|
|
|
ENST00000489643.6:n.833C>A
|
|
|
ENST00000554085.5:c.*497C>A
|
ENSP00000450419.1:n.*497C>A
|
|
ENST00000554550.5:c.*373C>A
|
ENSP00000451435.1:n.*373C>A
|
|
ENST00000554638.5:n.1225C>A
|
|
|
ENST00000555020.5:n.1214C>A
|
|
|
ENST00000555086.5:n.757C>A
|
|
|
ENST00000555754.1:n.98C>A
|
|
|
ENST00000556244.1:c.740C>A
|
|
|
ENST00000556278.1:c.432+371C>A
|
ENSP00000451792.1:n.432+371C>A
|
|
ENST00000557706.5:n.1315C>A
|
|
|
NM_000155.3:c.753C>A
|
NP_000146.2:p.Tyr251Ter
|
|
NM_001258332.1:c.426C>A
|
NP_001245261.1:p.Tyr142Ter
|
|
NM_000155.4:c.753C>A
MANE Select
|
NP_000146.2:p.Tyr251Ter
|
|
NM_001258332.2:c.426C>A
|
NP_001245261.1:p.Tyr142Ter
|
|