ENST00000496887.7:c.977G>T
|
ENSP00000434560.2:p.Cys326Phe
|
|
ENST00000646564.2:c.794G>T
|
ENSP00000495806.2:p.Cys265Phe
|
|
ENST00000155840.12:c.1334G>T
MANE Select
|
ENSP00000155840.2:p.Cys445Phe
|
|
ENST00000335475.6:c.953G>T
|
ENSP00000334497.5:p.Cys318Phe
|
|
ENST00000646564.1:c.440G>T
|
ENSP00000495806.1:p.Cys147Phe
|
|
ENST00000155840.9:c.1334G>T
|
ENSP00000155840.2:p.Cys445Phe
|
|
ENST00000335475.5:c.953G>T
|
ENSP00000334497.5:p.Cys318Phe
|
|
NM_000218.2:c.1334G>T , LRG_287t1:c.1334G>T
|
NP_000209.2:p.Cys445Phe
|
|
NM_181798.1:c.953G>T , LRG_287t2:c.953G>T
|
NP_861463.1:p.Cys318Phe
|
|
NM_000218.3:c.1334G>T
MANE Select
|
NP_000209.2:p.Cys445Phe
|
|