ENST00000476274.7:n.977T>A
|
|
|
ENST00000643029.1:c.*2152T>A
|
ENSP00000496586.1:n.*2152T>A
|
|
ENST00000643338.1:c.*2041T>A
|
ENSP00000495890.1:n.*2041T>A
|
|
ENST00000644144.2:c.477T>A
MANE Select
|
ENSP00000494600.1:p.Pro159=
|
|
ENST00000645007.1:c.*2401T>A
|
ENSP00000494773.1:n.*2401T>A
|
|
ENST00000646171.1:c.*510T>A
|
ENSP00000495484.1:n.*510T>A
|
|
ENST00000223836.10:c.525T>A
|
ENSP00000223836.10:p.Pro175=
|
|
ENST00000373156.5:c.477T>A
|
ENSP00000362249.1:p.Pro159=
|
|
ENST00000373176.5:c.477T>A
|
ENSP00000362271.1:p.Pro159=
|
|
ENST00000413016.5:c.299T>A
|
|
|
ENST00000550143.5:c.257T>A
|
ENSP00000449130.1:n.257T>A
|
|
XM_005251786.2:c.525T>A
|
XP_005251843.1:p.Pro175=
|
|
XM_011518348.1:c.477T>A
|
XP_011516650.1:p.Pro159=
|
|
XM_011518349.1:c.297T>A
|
XP_011516651.1:p.Pro99=
|
|
XM_017014428.1:c.477T>A
|
XP_016869917.1:p.Pro159=
|
|
XM_024447439.1:c.456T>A
|
XP_024303207.1:p.Pro152=
|
|
XM_024447440.1:c.297T>A
|
XP_024303208.1:p.Pro99=
|
|
NM_001318122.2:c.525T>A
|
NP_001305051.1:p.Pro175=
|
|
NM_000476.3:c.477T>A
MANE Select
|
NP_000467.1:p.Pro159=
|
|
NR_174625.1:n.3796T>A
|
|
|
NR_174626.1:n.3639T>A
|
|
|
NR_174627.1:n.3676T>A
|
|
|
NR_174628.1:n.3054T>A
|
|
|
NR_174629.1:n.2999T>A
|
|
|
NR_174630.1:n.3035T>A
|
|
|
NR_174631.1:n.2980T>A
|
|
|
NR_174632.1:n.3069T>A
|
|
|