ENST00000649046.1:c.12290G>A
MANE Select
|
ENSP00000496870.1:p.Gly4097Asp
|
|
ENST00000649153.1:c.3190G>A
|
|
|
ENST00000650252.1:c.1318G>A
|
ENSP00000496887.1:n.1318G>A
|
|
ENST00000263816.7:c.12290G>A
|
ENSP00000263816.3:p.Gly4097Asp
|
|
NM_004525.2:c.12290G>A
|
NP_004516.2:p.Gly4097Asp
|
|
XM_011511183.1:c.12161G>A
|
XP_011509485.1:p.Gly4054Asp
|
|
XM_011511184.1:c.10001G>A
|
XP_011509486.1:p.Gly3334Asp
|
|
NM_004525.3:c.12290G>A
MANE Select
|
NP_004516.2:p.Gly4097Asp
|
|
XM_011511183.3:c.12161G>A
|
XP_011509485.1:p.Gly4054Asp
|
|
XM_011511184.2:c.10001G>A
|
XP_011509486.1:p.Gly3334Asp
|
|