ENST00000496887.7:c.1427T>A
|
ENSP00000434560.2:p.Val476Glu
|
|
ENST00000646564.2:c.1244T>A
|
ENSP00000495806.2:p.Val415Glu
|
|
ENST00000155840.12:c.1784T>A
MANE Select
|
ENSP00000155840.2:p.Val595Glu
|
|
ENST00000335475.6:c.1403T>A
|
ENSP00000334497.5:p.Val468Glu
|
|
ENST00000526095.2:c.188T>A
|
ENSP00000494939.1:p.Val63Glu
|
|
ENST00000646564.1:c.890T>A
|
ENSP00000495806.1:p.Val297Glu
|
|
ENST00000155840.9:c.1784T>A
|
ENSP00000155840.2:p.Val595Glu
|
|
ENST00000335475.5:c.1403T>A
|
ENSP00000334497.5:p.Val468Glu
|
|
ENST00000526095.1:n.291T>A
|
|
|
NM_000218.2:c.1784T>A , LRG_287t1:c.1784T>A
|
NP_000209.2:p.Val595Glu
|
|
NM_181798.1:c.1403T>A , LRG_287t2:c.1403T>A
|
NP_861463.1:p.Val468Glu
|
|
NM_000218.3:c.1784T>A
MANE Select
|
NP_000209.2:p.Val595Glu
|
|