ENST00000267845.8:c.1724T>C
MANE Select
|
ENSP00000267845.3:p.Val575Ala
|
|
ENST00000267845.7:c.1724T>C
|
ENSP00000267845.3:p.Val575Ala
|
|
ENST00000543581.5:c.1625T>C
|
ENSP00000440252.1:p.Val542Ala
|
|
ENST00000559816.1:n.1468T>C
|
|
|
NM_001306146.1:c.1625T>C
|
NP_001293075.1:p.Val542Ala
|
|
NM_002112.3:c.1724T>C
|
NP_002103.2:p.Val575Ala
|
|
XM_011521479.1:c.1487T>C
|
XP_011519781.1:p.Val496Ala
|
|
XM_011521480.1:c.1292T>C
|
XP_011519782.1:p.Val431Ala
|
|
XM_017022094.1:c.1829T>C
|
XP_016877583.1:p.Val610Ala
|
|
XM_017022095.1:c.1730T>C
|
XP_016877584.1:p.Val577Ala
|
|
XM_017022096.1:c.1601T>C
|
XP_016877585.1:p.Val534Ala
|
|
XM_017022097.1:c.1592T>C
|
XP_016877586.1:p.Val531Ala
|
|
XM_017022098.1:c.1397T>C
|
XP_016877587.1:p.Val466Ala
|
|
NM_002112.4:c.1724T>C
MANE Select
|
NP_002103.2:p.Val575Ala
|
|
NM_001306146.2:c.1625T>C
|
NP_001293075.1:p.Val542Ala
|
|