ENST00000567697.2:n.3975G>A
|
|
|
ENST00000682393.1:c.*258-1478G>A
|
ENSP00000506774.1:n.*258-1478G>A
|
|
ENST00000683094.1:c.*262-1478G>A
|
ENSP00000508230.1:n.*262-1478G>A
|
|
ENST00000683274.1:c.*180-1478G>A
|
ENSP00000507262.1:n.*180-1478G>A
|
|
ENST00000683435.1:c.*703G>A
|
ENSP00000508092.1:n.*703G>A
|
|
ENST00000268261.9:c.*66G>A
MANE Select
|
ENSP00000268261.4:n.*66G>A
|
|
ENST00000268261.8:c.*66G>A
|
ENSP00000268261.4:n.*66G>A
|
|
ENST00000562025.1:n.341G>A
|
|
|
ENST00000562318.5:c.*529G>A
|
ENSP00000454395.1:n.*529G>A
|
|
ENST00000565221.5:c.*425G>A
|
ENSP00000457932.1:n.*425G>A
|
|
ENST00000566540.5:c.*429G>A
|
ENSP00000454284.1:n.*429G>A
|
|
ENST00000566604.5:c.*347G>A
|
ENSP00000456774.1:n.*347G>A
|
|
ENST00000567697.1:n.3975G>A
|
|
|
ENST00000569958.5:c.*66G>A
|
ENSP00000456302.1:n.*66G>A
|
|
ENST00000570076.5:c.*265G>A
|
ENSP00000456961.1:n.*265G>A
|
|
NM_000303.2:c.*66G>A
|
NP_000294.1:n.*66G>A
|
|
XM_005255374.3:c.*66G>A
|
XP_005255431.1:n.*66G>A
|
|
XM_011522538.1:c.640-7143G>A
|
XP_011520840.1:n.640-7143G>A
|
|
XM_005255374.4:c.*66G>A
|
XP_005255431.1:n.*66G>A
|
|
NM_000303.3:c.*66G>A
MANE Select
|
NP_000294.1:n.*66G>A
|
|