ENST00000496887.7:c.708G>T
|
ENSP00000434560.2:p.Trp236Cys
|
|
ENST00000646564.2:c.525G>T
|
ENSP00000495806.2:p.Trp175Cys
|
|
ENST00000155840.12:c.969G>T
MANE Select
|
ENSP00000155840.2:p.Trp323Cys
|
|
ENST00000335475.6:c.588G>T
|
ENSP00000334497.5:p.Trp196Cys
|
|
ENST00000646564.1:c.171G>T
|
ENSP00000495806.1:p.Trp57Cys
|
|
ENST00000155840.9:c.969G>T
|
ENSP00000155840.2:p.Trp323Cys
|
|
ENST00000335475.5:c.588G>T
|
ENSP00000334497.5:p.Trp196Cys
|
|
NM_000218.2:c.969G>T , LRG_287t1:c.969G>T
|
NP_000209.2:p.Trp323Cys
|
|
NM_181798.1:c.588G>T , LRG_287t2:c.588G>T
|
NP_861463.1:p.Trp196Cys
|
|
NM_000218.3:c.969G>T
MANE Select
|
NP_000209.2:p.Trp323Cys
|
|