ENST00000267845.8:c.1832G>T
MANE Select
|
ENSP00000267845.3:p.Arg611Met
|
|
ENST00000267845.7:c.1832G>T
|
ENSP00000267845.3:p.Arg611Met
|
|
ENST00000543581.5:c.1733G>T
|
ENSP00000440252.1:p.Arg578Met
|
|
ENST00000559816.1:n.1576G>T
|
|
|
NM_001306146.1:c.1733G>T
|
NP_001293075.1:p.Arg578Met
|
|
NM_002112.3:c.1832G>T
|
NP_002103.2:p.Arg611Met
|
|
XM_011521479.1:c.1595G>T
|
XP_011519781.1:p.Arg532Met
|
|
XM_011521480.1:c.1400G>T
|
XP_011519782.1:p.Arg467Met
|
|
XM_017022094.1:c.1937G>T
|
XP_016877583.1:p.Arg646Met
|
|
XM_017022095.1:c.1838G>T
|
XP_016877584.1:p.Arg613Met
|
|
XM_017022096.1:c.1709G>T
|
XP_016877585.1:p.Arg570Met
|
|
XM_017022097.1:c.1700G>T
|
XP_016877586.1:p.Arg567Met
|
|
XM_017022098.1:c.1505G>T
|
XP_016877587.1:p.Arg502Met
|
|
NM_002112.4:c.1832G>T
MANE Select
|
NP_002103.2:p.Arg611Met
|
|
NM_001306146.2:c.1733G>T
|
NP_001293075.1:p.Arg578Met
|
|