ENST00000527701.6:c.*1383G>T
|
ENSP00000435718.2:n.*1383G>T
|
|
ENST00000533313.6:c.*1337G>T
|
ENSP00000431843.2:n.*1337G>T
|
|
ENST00000616349.5:c.1411G>T
MANE Select
|
ENSP00000479524.2:p.Val471Phe
|
|
ENST00000332271.9:c.1411G>T
|
ENSP00000330031.5:p.Val471Phe
|
|
ENST00000527701.5:c.1084G>T
|
ENSP00000435718.1:p.Val362Phe
|
|
ENST00000532537.2:n.1832G>T
|
|
|
ENST00000533313.5:c.1084G>T
|
ENSP00000431843.1:p.Val362Phe
|
|
ENST00000616349.4:c.1411G>T
|
ENSP00000479524.1:p.Val471Phe
|
|
NM_001008496.3:c.1411G>T
|
NP_001008496.2:p.Val471Phe
|
|
NM_001255975.1:c.1411G>T
MANE Select
|
NP_001242904.1:p.Val471Phe
|
|
NR_045648.1:n.2042G>T
|
|
|
NR_045649.2:n.1915G>T
|
|
|