ENST00000426263.10:c.272G>A
MANE Select
|
ENSP00000416293.2:p.Gly91Asp
|
|
ENST00000674765.1:c.272G>A
|
ENSP00000501811.1:p.Gly91Asp
|
|
ENST00000675112.1:n.295G>A
|
|
|
ENST00000676254.1:n.721G>A
|
|
|
ENST00000372500.4:c.176G>A
|
ENSP00000361578.4:p.Gly59Asp
|
|
ENST00000415851.6:n.489G>A
|
|
|
ENST00000426263.7:c.272G>A
|
ENSP00000416293.2:p.Gly91Asp
|
|
ENST00000439722.2:c.77G>A
|
ENSP00000395521.2:p.Gly26Asp
|
|
ENST00000475162.3:c.171G>A
|
|
|
ENST00000625233.2:n.480G>A
|
|
|
ENST00000630287.2:c.272G>A
|
ENSP00000486694.1:p.Gly91Asp
|
|
NM_006516.2:c.272G>A
|
NP_006507.2:p.Gly91Asp
|
|
NM_006516.3:c.272G>A
|
NP_006507.2:p.Gly91Asp
|
|
NM_006516.4:c.272G>A
MANE Select
|
NP_006507.2:p.Gly91Asp
|
|