ENST00000267845.8:c.1791A>T
MANE Select
|
ENSP00000267845.3:p.Pro597=
|
|
ENST00000267845.7:c.1791A>T
|
ENSP00000267845.3:p.Pro597=
|
|
ENST00000543581.5:c.1692A>T
|
ENSP00000440252.1:p.Pro564=
|
|
ENST00000559816.1:n.1535A>T
|
|
|
NM_001306146.1:c.1692A>T
|
NP_001293075.1:p.Pro564=
|
|
NM_002112.3:c.1791A>T
|
NP_002103.2:p.Pro597=
|
|
XM_011521479.1:c.1554A>T
|
XP_011519781.1:p.Pro518=
|
|
XM_011521480.1:c.1359A>T
|
XP_011519782.1:p.Pro453=
|
|
XM_017022094.1:c.1896A>T
|
XP_016877583.1:p.Pro632=
|
|
XM_017022095.1:c.1797A>T
|
XP_016877584.1:p.Pro599=
|
|
XM_017022096.1:c.1668A>T
|
XP_016877585.1:p.Pro556=
|
|
XM_017022097.1:c.1659A>T
|
XP_016877586.1:p.Pro553=
|
|
XM_017022098.1:c.1464A>T
|
XP_016877587.1:p.Pro488=
|
|
NM_002112.4:c.1791A>T
MANE Select
|
NP_002103.2:p.Pro597=
|
|
NM_001306146.2:c.1692A>T
|
NP_001293075.1:p.Pro564=
|
|