ENST00000267845.8:c.1706T>A
MANE Select
|
ENSP00000267845.3:p.Leu569Gln
|
|
ENST00000267845.7:c.1706T>A
|
ENSP00000267845.3:p.Leu569Gln
|
|
ENST00000543581.5:c.1607T>A
|
ENSP00000440252.1:p.Leu536Gln
|
|
ENST00000559816.1:n.1450T>A
|
|
|
NM_001306146.1:c.1607T>A
|
NP_001293075.1:p.Leu536Gln
|
|
NM_002112.3:c.1706T>A
|
NP_002103.2:p.Leu569Gln
|
|
XM_011521479.1:c.1469T>A
|
XP_011519781.1:p.Leu490Gln
|
|
XM_011521480.1:c.1274T>A
|
XP_011519782.1:p.Leu425Gln
|
|
XM_017022094.1:c.1811T>A
|
XP_016877583.1:p.Leu604Gln
|
|
XM_017022095.1:c.1712T>A
|
XP_016877584.1:p.Leu571Gln
|
|
XM_017022096.1:c.1583T>A
|
XP_016877585.1:p.Leu528Gln
|
|
XM_017022097.1:c.1574T>A
|
XP_016877586.1:p.Leu525Gln
|
|
XM_017022098.1:c.1379T>A
|
XP_016877587.1:p.Leu460Gln
|
|
NM_002112.4:c.1706T>A
MANE Select
|
NP_002103.2:p.Leu569Gln
|
|
NM_001306146.2:c.1607T>A
|
NP_001293075.1:p.Leu536Gln
|
|