ENST00000496887.7:c.1003G>T
|
ENSP00000434560.2:p.Asp335Tyr
|
|
ENST00000646564.2:c.820G>T
|
ENSP00000495806.2:p.Asp274Tyr
|
|
ENST00000155840.12:c.1360G>T
MANE Select
|
ENSP00000155840.2:p.Asp454Tyr
|
|
ENST00000335475.6:c.979G>T
|
ENSP00000334497.5:p.Asp327Tyr
|
|
ENST00000646564.1:c.466G>T
|
ENSP00000495806.1:p.Asp156Tyr
|
|
ENST00000155840.9:c.1360G>T
|
ENSP00000155840.2:p.Asp454Tyr
|
|
ENST00000335475.5:c.979G>T
|
ENSP00000334497.5:p.Asp327Tyr
|
|
NM_000218.2:c.1360G>T , LRG_287t1:c.1360G>T
|
NP_000209.2:p.Asp454Tyr
|
|
NM_181798.1:c.979G>T , LRG_287t2:c.979G>T
|
NP_861463.1:p.Asp327Tyr
|
|
NM_000218.3:c.1360G>T
MANE Select
|
NP_000209.2:p.Asp454Tyr
|
|