ENST00000496887.7:c.713G>T
|
ENSP00000434560.2:p.Gly238Val
|
|
ENST00000646564.2:c.530G>T
|
ENSP00000495806.2:p.Gly177Val
|
|
ENST00000155840.12:c.974G>T
MANE Select
|
ENSP00000155840.2:p.Gly325Val
|
|
ENST00000335475.6:c.593G>T
|
ENSP00000334497.5:p.Gly198Val
|
|
ENST00000646564.1:c.176G>T
|
ENSP00000495806.1:p.Gly59Val
|
|
ENST00000155840.9:c.974G>T
|
ENSP00000155840.2:p.Gly325Val
|
|
ENST00000335475.5:c.593G>T
|
ENSP00000334497.5:p.Gly198Val
|
|
NM_000218.2:c.974G>T , LRG_287t1:c.974G>T
|
NP_000209.2:p.Gly325Val
|
|
NM_181798.1:c.593G>T , LRG_287t2:c.593G>T
|
NP_861463.1:p.Gly198Val
|
|
NM_000218.3:c.974G>T
MANE Select
|
NP_000209.2:p.Gly325Val
|
|