ENST00000267845.8:c.1838G>A
MANE Select
|
ENSP00000267845.3:p.Arg613Lys
|
|
ENST00000267845.7:c.1838G>A
|
ENSP00000267845.3:p.Arg613Lys
|
|
ENST00000543581.5:c.1739G>A
|
ENSP00000440252.1:p.Arg580Lys
|
|
ENST00000559816.1:n.1582G>A
|
|
|
NM_001306146.1:c.1739G>A
|
NP_001293075.1:p.Arg580Lys
|
|
NM_002112.3:c.1838G>A
|
NP_002103.2:p.Arg613Lys
|
|
XM_011521479.1:c.1601G>A
|
XP_011519781.1:p.Arg534Lys
|
|
XM_011521480.1:c.1406G>A
|
XP_011519782.1:p.Arg469Lys
|
|
XM_017022094.1:c.1943G>A
|
XP_016877583.1:p.Arg648Lys
|
|
XM_017022095.1:c.1844G>A
|
XP_016877584.1:p.Arg615Lys
|
|
XM_017022096.1:c.1715G>A
|
XP_016877585.1:p.Arg572Lys
|
|
XM_017022097.1:c.1706G>A
|
XP_016877586.1:p.Arg569Lys
|
|
XM_017022098.1:c.1511G>A
|
XP_016877587.1:p.Arg504Lys
|
|
NM_002112.4:c.1838G>A
MANE Select
|
NP_002103.2:p.Arg613Lys
|
|
NM_001306146.2:c.1739G>A
|
NP_001293075.1:p.Arg580Lys
|
|