ENST00000496887.7:c.1021G>C
|
ENSP00000434560.2:p.Gly341Arg
|
|
ENST00000646564.2:c.838G>C
|
ENSP00000495806.2:p.Gly280Arg
|
|
ENST00000155840.12:c.1378G>C
MANE Select
|
ENSP00000155840.2:p.Gly460Arg
|
|
ENST00000335475.6:c.997G>C
|
ENSP00000334497.5:p.Gly333Arg
|
|
ENST00000646564.1:c.484G>C
|
ENSP00000495806.1:p.Gly162Arg
|
|
ENST00000155840.9:c.1378G>C
|
ENSP00000155840.2:p.Gly460Arg
|
|
ENST00000335475.5:c.997G>C
|
ENSP00000334497.5:p.Gly333Arg
|
|
NM_000218.2:c.1378G>C , LRG_287t1:c.1378G>C
|
NP_000209.2:p.Gly460Arg
|
|
NM_181798.1:c.997G>C , LRG_287t2:c.997G>C
|
NP_861463.1:p.Gly333Arg
|
|
NM_000218.3:c.1378G>C
MANE Select
|
NP_000209.2:p.Gly460Arg
|
|