ENST00000496887.7:c.827A>C
|
ENSP00000434560.2:p.Tyr276Ser
|
|
ENST00000646564.2:c.644A>C
|
ENSP00000495806.2:p.Tyr215Ser
|
|
ENST00000155840.12:c.1184A>C
MANE Select
|
ENSP00000155840.2:p.Tyr395Ser
|
|
ENST00000335475.6:c.803A>C
|
ENSP00000334497.5:p.Tyr268Ser
|
|
ENST00000646564.1:c.290A>C
|
ENSP00000495806.1:p.Tyr97Ser
|
|
ENST00000155840.9:c.1184A>C
|
ENSP00000155840.2:p.Tyr395Ser
|
|
ENST00000335475.5:c.803A>C
|
ENSP00000334497.5:p.Tyr268Ser
|
|
NM_000218.2:c.1184A>C , LRG_287t1:c.1184A>C
|
NP_000209.2:p.Tyr395Ser
|
|
NM_181798.1:c.803A>C , LRG_287t2:c.803A>C
|
NP_861463.1:p.Tyr268Ser
|
|
NM_000218.3:c.1184A>C
MANE Select
|
NP_000209.2:p.Tyr395Ser
|
|