ENST00000267845.8:c.1980C>T
MANE Select
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ENSP00000267845.3:p.Ala660=
|
|
ENST00000267845.7:c.1980C>T
|
ENSP00000267845.3:p.Ala660=
|
|
ENST00000543581.5:c.1881C>T
|
ENSP00000440252.1:p.Ala627=
|
|
ENST00000559816.1:n.1724C>T
|
|
|
NM_001306146.1:c.1881C>T
|
NP_001293075.1:p.Ala627=
|
|
NM_002112.3:c.1980C>T
|
NP_002103.2:p.Ala660=
|
|
XM_011521479.1:c.1743C>T
|
XP_011519781.1:p.Ala581=
|
|
XM_011521480.1:c.1548C>T
|
XP_011519782.1:p.Ala516=
|
|
XM_017022094.1:c.2085C>T
|
XP_016877583.1:p.Ala695=
|
|
XM_017022095.1:c.1986C>T
|
XP_016877584.1:p.Ala662=
|
|
XM_017022096.1:c.1857C>T
|
XP_016877585.1:p.Ala619=
|
|
XM_017022097.1:c.1848C>T
|
XP_016877586.1:p.Ala616=
|
|
XM_017022098.1:c.1653C>T
|
XP_016877587.1:p.Ala551=
|
|
NM_002112.4:c.1980C>T
MANE Select
|
NP_002103.2:p.Ala660=
|
|
NM_001306146.2:c.1881C>T
|
NP_001293075.1:p.Ala627=
|
|