ENST00000267845.8:c.1952T>G
MANE Select
|
ENSP00000267845.3:p.Leu651Arg
|
|
ENST00000267845.7:c.1952T>G
|
ENSP00000267845.3:p.Leu651Arg
|
|
ENST00000543581.5:c.1853T>G
|
ENSP00000440252.1:p.Leu618Arg
|
|
ENST00000559816.1:n.1696T>G
|
|
|
NM_001306146.1:c.1853T>G
|
NP_001293075.1:p.Leu618Arg
|
|
NM_002112.3:c.1952T>G
|
NP_002103.2:p.Leu651Arg
|
|
XM_011521479.1:c.1715T>G
|
XP_011519781.1:p.Leu572Arg
|
|
XM_011521480.1:c.1520T>G
|
XP_011519782.1:p.Leu507Arg
|
|
XM_017022094.1:c.2057T>G
|
XP_016877583.1:p.Leu686Arg
|
|
XM_017022095.1:c.1958T>G
|
XP_016877584.1:p.Leu653Arg
|
|
XM_017022096.1:c.1829T>G
|
XP_016877585.1:p.Leu610Arg
|
|
XM_017022097.1:c.1820T>G
|
XP_016877586.1:p.Leu607Arg
|
|
XM_017022098.1:c.1625T>G
|
XP_016877587.1:p.Leu542Arg
|
|
NM_002112.4:c.1952T>G
MANE Select
|
NP_002103.2:p.Leu651Arg
|
|
NM_001306146.2:c.1853T>G
|
NP_001293075.1:p.Leu618Arg
|
|