ENST00000267845.8:c.1837A>T
MANE Select
|
ENSP00000267845.3:p.Arg613Ter
|
|
ENST00000267845.7:c.1837A>T
|
ENSP00000267845.3:p.Arg613Ter
|
|
ENST00000543581.5:c.1738A>T
|
ENSP00000440252.1:p.Arg580Ter
|
|
ENST00000559816.1:n.1581A>T
|
|
|
NM_001306146.1:c.1738A>T
|
NP_001293075.1:p.Arg580Ter
|
|
NM_002112.3:c.1837A>T
|
NP_002103.2:p.Arg613Ter
|
|
XM_011521479.1:c.1600A>T
|
XP_011519781.1:p.Arg534Ter
|
|
XM_011521480.1:c.1405A>T
|
XP_011519782.1:p.Arg469Ter
|
|
XM_017022094.1:c.1942A>T
|
XP_016877583.1:p.Arg648Ter
|
|
XM_017022095.1:c.1843A>T
|
XP_016877584.1:p.Arg615Ter
|
|
XM_017022096.1:c.1714A>T
|
XP_016877585.1:p.Arg572Ter
|
|
XM_017022097.1:c.1705A>T
|
XP_016877586.1:p.Arg569Ter
|
|
XM_017022098.1:c.1510A>T
|
XP_016877587.1:p.Arg504Ter
|
|
NM_002112.4:c.1837A>T
MANE Select
|
NP_002103.2:p.Arg613Ter
|
|
NM_001306146.2:c.1738A>T
|
NP_001293075.1:p.Arg580Ter
|
|