ENST00000496887.7:c.1198C>T
|
ENSP00000434560.2:p.Arg400Cys
|
|
ENST00000646564.2:c.1015C>T
|
ENSP00000495806.2:p.Arg339Cys
|
|
ENST00000155840.12:c.1555C>T
MANE Select
|
ENSP00000155840.2:p.Arg519Cys
|
|
ENST00000335475.6:c.1174C>T
|
ENSP00000334497.5:p.Arg392Cys
|
|
ENST00000646564.1:c.661C>T
|
ENSP00000495806.1:p.Arg221Cys
|
|
ENST00000155840.9:c.1555C>T
|
ENSP00000155840.2:p.Arg519Cys
|
|
ENST00000335475.5:c.1174C>T
|
ENSP00000334497.5:p.Arg392Cys
|
|
NM_000218.2:c.1555C>T , LRG_287t1:c.1555C>T
|
NP_000209.2:p.Arg519Cys
|
|
NM_181798.1:c.1174C>T , LRG_287t2:c.1174C>T
|
NP_861463.1:p.Arg392Cys
|
|
NM_000218.3:c.1555C>T
MANE Select
|
NP_000209.2:p.Arg519Cys
|
|