ENST00000267845.8:c.1702T>A
MANE Select
|
ENSP00000267845.3:p.Phe568Ile
|
|
ENST00000267845.7:c.1702T>A
|
ENSP00000267845.3:p.Phe568Ile
|
|
ENST00000543581.5:c.1603T>A
|
ENSP00000440252.1:p.Phe535Ile
|
|
ENST00000559816.1:n.1446T>A
|
|
|
NM_001306146.1:c.1603T>A
|
NP_001293075.1:p.Phe535Ile
|
|
NM_002112.3:c.1702T>A
|
NP_002103.2:p.Phe568Ile
|
|
XM_011521479.1:c.1465T>A
|
XP_011519781.1:p.Phe489Ile
|
|
XM_011521480.1:c.1270T>A
|
XP_011519782.1:p.Phe424Ile
|
|
XM_017022094.1:c.1807T>A
|
XP_016877583.1:p.Phe603Ile
|
|
XM_017022095.1:c.1708T>A
|
XP_016877584.1:p.Phe570Ile
|
|
XM_017022096.1:c.1579T>A
|
XP_016877585.1:p.Phe527Ile
|
|
XM_017022097.1:c.1570T>A
|
XP_016877586.1:p.Phe524Ile
|
|
XM_017022098.1:c.1375T>A
|
XP_016877587.1:p.Phe459Ile
|
|
NM_002112.4:c.1702T>A
MANE Select
|
NP_002103.2:p.Phe568Ile
|
|
NM_001306146.2:c.1603T>A
|
NP_001293075.1:p.Phe535Ile
|
|