ENST00000267845.8:c.1739A>T
MANE Select
|
ENSP00000267845.3:p.Lys580Met
|
|
ENST00000267845.7:c.1739A>T
|
ENSP00000267845.3:p.Lys580Met
|
|
ENST00000543581.5:c.1640A>T
|
ENSP00000440252.1:p.Lys547Met
|
|
ENST00000559816.1:n.1483A>T
|
|
|
NM_001306146.1:c.1640A>T
|
NP_001293075.1:p.Lys547Met
|
|
NM_002112.3:c.1739A>T
|
NP_002103.2:p.Lys580Met
|
|
XM_011521479.1:c.1502A>T
|
XP_011519781.1:p.Lys501Met
|
|
XM_011521480.1:c.1307A>T
|
XP_011519782.1:p.Lys436Met
|
|
XM_017022094.1:c.1844A>T
|
XP_016877583.1:p.Lys615Met
|
|
XM_017022095.1:c.1745A>T
|
XP_016877584.1:p.Lys582Met
|
|
XM_017022096.1:c.1616A>T
|
XP_016877585.1:p.Lys539Met
|
|
XM_017022097.1:c.1607A>T
|
XP_016877586.1:p.Lys536Met
|
|
XM_017022098.1:c.1412A>T
|
XP_016877587.1:p.Lys471Met
|
|
NM_002112.4:c.1739A>T
MANE Select
|
NP_002103.2:p.Lys580Met
|
|
NM_001306146.2:c.1640A>T
|
NP_001293075.1:p.Lys547Met
|
|