ENST00000380776.5:n.204G>T
|
|
|
ENST00000496887.7:c.146G>T
|
ENSP00000434560.2:p.Cys49Phe
|
|
ENST00000646564.2:c.407G>T
|
ENSP00000495806.2:p.Cys136Phe
|
|
ENST00000155840.12:c.407G>T
MANE Select
|
ENSP00000155840.2:p.Cys136Phe
|
|
ENST00000335475.6:c.26G>T
|
ENSP00000334497.5:p.Cys9Phe
|
|
ENST00000646564.1:c.53G>T
|
ENSP00000495806.1:p.Cys18Phe
|
|
ENST00000155840.9:c.407G>T
|
ENSP00000155840.2:p.Cys136Phe
|
|
ENST00000335475.5:c.26G>T
|
ENSP00000334497.5:p.Cys9Phe
|
|
ENST00000345015.4:n.276G>T
|
|
|
ENST00000380776.4:c.197G>T
|
ENSP00000370153.4:p.Cys66Phe
|
|
ENST00000496887.6:c.146G>T
|
ENSP00000434560.1:p.Cys49Phe
|
|
NM_000218.2:c.407G>T , LRG_287t1:c.407G>T
|
NP_000209.2:p.Cys136Phe
|
|
NM_181798.1:c.26G>T , LRG_287t2:c.26G>T
|
NP_861463.1:p.Cys9Phe
|
|
NM_000218.3:c.407G>T
MANE Select
|
NP_000209.2:p.Cys136Phe
|
|