ENST00000267845.8:c.1832G>C
MANE Select
|
ENSP00000267845.3:p.Arg611Thr
|
|
ENST00000267845.7:c.1832G>C
|
ENSP00000267845.3:p.Arg611Thr
|
|
ENST00000543581.5:c.1733G>C
|
ENSP00000440252.1:p.Arg578Thr
|
|
ENST00000559816.1:n.1576G>C
|
|
|
NM_001306146.1:c.1733G>C
|
NP_001293075.1:p.Arg578Thr
|
|
NM_002112.3:c.1832G>C
|
NP_002103.2:p.Arg611Thr
|
|
XM_011521479.1:c.1595G>C
|
XP_011519781.1:p.Arg532Thr
|
|
XM_011521480.1:c.1400G>C
|
XP_011519782.1:p.Arg467Thr
|
|
XM_017022094.1:c.1937G>C
|
XP_016877583.1:p.Arg646Thr
|
|
XM_017022095.1:c.1838G>C
|
XP_016877584.1:p.Arg613Thr
|
|
XM_017022096.1:c.1709G>C
|
XP_016877585.1:p.Arg570Thr
|
|
XM_017022097.1:c.1700G>C
|
XP_016877586.1:p.Arg567Thr
|
|
XM_017022098.1:c.1505G>C
|
XP_016877587.1:p.Arg502Thr
|
|
NM_002112.4:c.1832G>C
MANE Select
|
NP_002103.2:p.Arg611Thr
|
|
NM_001306146.2:c.1733G>C
|
NP_001293075.1:p.Arg578Thr
|
|