ENST00000267845.8:c.1793T>A
MANE Select
|
ENSP00000267845.3:p.Leu598Gln
|
|
ENST00000267845.7:c.1793T>A
|
ENSP00000267845.3:p.Leu598Gln
|
|
ENST00000543581.5:c.1694T>A
|
ENSP00000440252.1:p.Leu565Gln
|
|
ENST00000559816.1:n.1537T>A
|
|
|
NM_001306146.1:c.1694T>A
|
NP_001293075.1:p.Leu565Gln
|
|
NM_002112.3:c.1793T>A
|
NP_002103.2:p.Leu598Gln
|
|
XM_011521479.1:c.1556T>A
|
XP_011519781.1:p.Leu519Gln
|
|
XM_011521480.1:c.1361T>A
|
XP_011519782.1:p.Leu454Gln
|
|
XM_017022094.1:c.1898T>A
|
XP_016877583.1:p.Leu633Gln
|
|
XM_017022095.1:c.1799T>A
|
XP_016877584.1:p.Leu600Gln
|
|
XM_017022096.1:c.1670T>A
|
XP_016877585.1:p.Leu557Gln
|
|
XM_017022097.1:c.1661T>A
|
XP_016877586.1:p.Leu554Gln
|
|
XM_017022098.1:c.1466T>A
|
XP_016877587.1:p.Leu489Gln
|
|
NM_002112.4:c.1793T>A
MANE Select
|
NP_002103.2:p.Leu598Gln
|
|
NM_001306146.2:c.1694T>A
|
NP_001293075.1:p.Leu565Gln
|
|