ENST00000496887.7:c.598G>A
|
ENSP00000434560.2:p.Ala200Thr
|
|
ENST00000646564.2:c.478-10511G>A
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ENSP00000495806.2:n.478-10511G>A
|
|
ENST00000155840.12:c.859G>A
MANE Select
|
ENSP00000155840.2:p.Ala287Thr
|
|
ENST00000335475.6:c.478G>A
|
ENSP00000334497.5:p.Ala160Thr
|
|
ENST00000646564.1:c.124-10511G>A
|
ENSP00000495806.1:n.124-10511G>A
|
|
ENST00000155840.9:c.859G>A
|
ENSP00000155840.2:p.Ala287Thr
|
|
ENST00000335475.5:c.478G>A
|
ENSP00000334497.5:p.Ala160Thr
|
|
NM_000218.2:c.859G>A , LRG_287t1:c.859G>A
|
NP_000209.2:p.Ala287Thr
|
|
NM_181798.1:c.478G>A , LRG_287t2:c.478G>A
|
NP_861463.1:p.Ala160Thr
|
|
NM_000218.3:c.859G>A
MANE Select
|
NP_000209.2:p.Ala287Thr
|
|