ENST00000354280.9:c.49G=
(EPPIN)
MANE Select
|
ENSP00000361746.4:p.Ala17=
|
|
ENST00000651288.1:c.49G=
(EPPIN-WFDC6)
|
ENSP00000498632.1:p.Ala17=
|
|
ENST00000354280.8:c.49G=
(EPPIN)
|
ENSP00000361746.3:p.Ala17=
|
|
ENST00000409554.1:c.49G=
(EPPIN)
|
ENSP00000387153.1:p.Ala17=
|
|
ENST00000496898.1:n.49G=
(EPPIN)
|
|
|
ENST00000504988.1:c.49G=
(EPPIN-WFDC6)
|
ENSP00000424176.1:p.Ala17=
|
|
NM_001198986.1:c.49G=
(EPPIN-WFDC6)
|
NP_001185915.1:p.Ala17=
|
|
NM_001302861.1:c.49G=
(EPPIN)
|
NP_001289790.1:p.Ala17=
|
|
NM_020398.3:c.49G=
(EPPIN)
|
NP_065131.1:p.Ala17=
|
|
NM_001198986.2:c.49G=
(EPPIN-WFDC6)
|
NP_001185915.1:p.Ala17=
|
|
NM_001302861.2:c.49G=
(EPPIN)
|
NP_001289790.1:p.Ala17=
|
|
NM_020398.4:c.49G=
(EPPIN)
MANE Select
|
NP_065131.1:p.Ala17=
|
|