ENST00000496887.7:c.771+1686T>G
|
ENSP00000434560.2:n.771+1686T>G
|
|
ENST00000646564.2:c.588+1686T>G
|
ENSP00000495806.2:n.588+1686T>G
|
|
ENST00000155840.12:c.1052T>G
MANE Select
|
ENSP00000155840.2:p.Phe351Cys
|
|
ENST00000335475.6:c.671T>G
|
ENSP00000334497.5:p.Phe224Cys
|
|
ENST00000646564.1:c.234+1686T>G
|
ENSP00000495806.1:n.234+1686T>G
|
|
ENST00000155840.9:c.1052T>G
|
ENSP00000155840.2:p.Phe351Cys
|
|
ENST00000335475.5:c.671T>G
|
ENSP00000334497.5:p.Phe224Cys
|
|
NM_000218.2:c.1052T>G , LRG_287t1:c.1052T>G
|
NP_000209.2:p.Phe351Cys
|
|
NM_181798.1:c.671T>G , LRG_287t2:c.671T>G
|
NP_861463.1:p.Phe224Cys
|
|
NM_000218.3:c.1052T>G
MANE Select
|
NP_000209.2:p.Phe351Cys
|
|