ENST00000691183.1:c.*323C>T
|
ENSP00000509954.1:n.*323C>T
|
|
ENST00000378842.8:c.735C>T
MANE Select
|
ENSP00000368119.4:p.Phe245=
|
|
ENST00000378842.7:c.735C>T
|
ENSP00000368119.3:p.Phe245=
|
|
ENST00000450095.6:c.408C>T
|
ENSP00000401956.2:p.Phe136=
|
|
ENST00000473506.6:c.*323C>T
|
ENSP00000432839.2:n.*323C>T
|
|
ENST00000473529.5:n.894C>T
|
|
|
ENST00000487381.5:n.1425C>T
|
|
|
ENST00000489643.6:n.815C>T
|
|
|
ENST00000554085.5:c.*479C>T
|
ENSP00000450419.1:n.*479C>T
|
|
ENST00000554550.5:c.*355C>T
|
ENSP00000451435.1:n.*355C>T
|
|
ENST00000554638.5:n.1207C>T
|
|
|
ENST00000555020.5:n.1196C>T
|
|
|
ENST00000555086.5:n.739C>T
|
|
|
ENST00000555754.1:n.80C>T
|
|
|
ENST00000556244.1:c.722C>T
|
|
|
ENST00000556278.1:c.432+353C>T
|
ENSP00000451792.1:n.432+353C>T
|
|
ENST00000557706.5:n.1297C>T
|
|
|
NM_000155.3:c.735C>T
|
NP_000146.2:p.Phe245=
|
|
NM_001258332.1:c.408C>T
|
NP_001245261.1:p.Phe136=
|
|
NM_000155.4:c.735C>T
MANE Select
|
NP_000146.2:p.Phe245=
|
|
NM_001258332.2:c.408C>T
|
NP_001245261.1:p.Phe136=
|
|