ENST00000496887.7:c.668T>C
|
ENSP00000434560.2:p.Val223Ala
|
|
ENST00000646564.2:c.485T>C
|
ENSP00000495806.2:p.Val162Ala
|
|
ENST00000155840.12:c.929T>C
MANE Select
|
ENSP00000155840.2:p.Val310Ala
|
|
ENST00000335475.6:c.548T>C
|
ENSP00000334497.5:p.Val183Ala
|
|
ENST00000646564.1:c.131T>C
|
ENSP00000495806.1:p.Val44Ala
|
|
ENST00000155840.9:c.929T>C
|
ENSP00000155840.2:p.Val310Ala
|
|
ENST00000335475.5:c.548T>C
|
ENSP00000334497.5:p.Val183Ala
|
|
NM_000218.2:c.929T>C , LRG_287t1:c.929T>C
|
NP_000209.2:p.Val310Ala
|
|
NM_181798.1:c.548T>C , LRG_287t2:c.548T>C
|
NP_861463.1:p.Val183Ala
|
|
NM_000218.3:c.929T>C
MANE Select
|
NP_000209.2:p.Val310Ala
|
|