ENST00000496887.7:c.829A>T
|
ENSP00000434560.2:p.Ile277Phe
|
|
ENST00000646564.2:c.646A>T
|
ENSP00000495806.2:p.Ile216Phe
|
|
ENST00000155840.12:c.1186A>T
MANE Select
|
ENSP00000155840.2:p.Ile396Phe
|
|
ENST00000335475.6:c.805A>T
|
ENSP00000334497.5:p.Ile269Phe
|
|
ENST00000646564.1:c.292A>T
|
ENSP00000495806.1:p.Ile98Phe
|
|
ENST00000155840.9:c.1186A>T
|
ENSP00000155840.2:p.Ile396Phe
|
|
ENST00000335475.5:c.805A>T
|
ENSP00000334497.5:p.Ile269Phe
|
|
NM_000218.2:c.1186A>T , LRG_287t1:c.1186A>T
|
NP_000209.2:p.Ile396Phe
|
|
NM_181798.1:c.805A>T , LRG_287t2:c.805A>T
|
NP_861463.1:p.Ile269Phe
|
|
NM_000218.3:c.1186A>T
MANE Select
|
NP_000209.2:p.Ile396Phe
|
|