ENST00000267845.8:c.1835T>A
MANE Select
|
ENSP00000267845.3:p.Val612Asp
|
|
ENST00000267845.7:c.1835T>A
|
ENSP00000267845.3:p.Val612Asp
|
|
ENST00000543581.5:c.1736T>A
|
ENSP00000440252.1:p.Val579Asp
|
|
ENST00000559816.1:n.1579T>A
|
|
|
NM_001306146.1:c.1736T>A
|
NP_001293075.1:p.Val579Asp
|
|
NM_002112.3:c.1835T>A
|
NP_002103.2:p.Val612Asp
|
|
XM_011521479.1:c.1598T>A
|
XP_011519781.1:p.Val533Asp
|
|
XM_011521480.1:c.1403T>A
|
XP_011519782.1:p.Val468Asp
|
|
XM_017022094.1:c.1940T>A
|
XP_016877583.1:p.Val647Asp
|
|
XM_017022095.1:c.1841T>A
|
XP_016877584.1:p.Val614Asp
|
|
XM_017022096.1:c.1712T>A
|
XP_016877585.1:p.Val571Asp
|
|
XM_017022097.1:c.1703T>A
|
XP_016877586.1:p.Val568Asp
|
|
XM_017022098.1:c.1508T>A
|
XP_016877587.1:p.Val503Asp
|
|
NM_002112.4:c.1835T>A
MANE Select
|
NP_002103.2:p.Val612Asp
|
|
NM_001306146.2:c.1736T>A
|
NP_001293075.1:p.Val579Asp
|
|