ENST00000267845.8:c.1773A>C
MANE Select
|
ENSP00000267845.3:p.Pro591=
|
|
ENST00000267845.7:c.1773A>C
|
ENSP00000267845.3:p.Pro591=
|
|
ENST00000543581.5:c.1674A>C
|
ENSP00000440252.1:p.Pro558=
|
|
ENST00000559816.1:n.1517A>C
|
|
|
NM_001306146.1:c.1674A>C
|
NP_001293075.1:p.Pro558=
|
|
NM_002112.3:c.1773A>C
|
NP_002103.2:p.Pro591=
|
|
XM_011521479.1:c.1536A>C
|
XP_011519781.1:p.Pro512=
|
|
XM_011521480.1:c.1341A>C
|
XP_011519782.1:p.Pro447=
|
|
XM_017022094.1:c.1878A>C
|
XP_016877583.1:p.Pro626=
|
|
XM_017022095.1:c.1779A>C
|
XP_016877584.1:p.Pro593=
|
|
XM_017022096.1:c.1650A>C
|
XP_016877585.1:p.Pro550=
|
|
XM_017022097.1:c.1641A>C
|
XP_016877586.1:p.Pro547=
|
|
XM_017022098.1:c.1446A>C
|
XP_016877587.1:p.Pro482=
|
|
NM_002112.4:c.1773A>C
MANE Select
|
NP_002103.2:p.Pro591=
|
|
NM_001306146.2:c.1674A>C
|
NP_001293075.1:p.Pro558=
|
|