ENST00000496887.7:c.1016T>C
|
ENSP00000434560.2:p.Val339Ala
|
|
ENST00000646564.2:c.833T>C
|
ENSP00000495806.2:p.Val278Ala
|
|
ENST00000155840.12:c.1373T>C
MANE Select
|
ENSP00000155840.2:p.Val458Ala
|
|
ENST00000335475.6:c.992T>C
|
ENSP00000334497.5:p.Val331Ala
|
|
ENST00000646564.1:c.479T>C
|
ENSP00000495806.1:p.Val160Ala
|
|
ENST00000155840.9:c.1373T>C
|
ENSP00000155840.2:p.Val458Ala
|
|
ENST00000335475.5:c.992T>C
|
ENSP00000334497.5:p.Val331Ala
|
|
NM_000218.2:c.1373T>C , LRG_287t1:c.1373T>C
|
NP_000209.2:p.Val458Ala
|
|
NM_181798.1:c.992T>C , LRG_287t2:c.992T>C
|
NP_861463.1:p.Val331Ala
|
|
NM_000218.3:c.1373T>C
MANE Select
|
NP_000209.2:p.Val458Ala
|
|