ENST00000426263.10:c.502A>G
MANE Select
|
ENSP00000416293.2:p.Ile168Val
|
|
ENST00000674765.1:c.502A>G
|
ENSP00000501811.1:p.Ile168Val
|
|
ENST00000675112.1:n.525A>G
|
|
|
ENST00000676254.1:n.951A>G
|
|
|
ENST00000426263.7:c.502A>G
|
ENSP00000416293.2:p.Ile168Val
|
|
ENST00000439722.2:c.381A>G
|
ENSP00000395521.2:n.381A>G
|
|
ENST00000475162.3:c.401A>G
|
|
|
ENST00000625233.2:n.710A>G
|
|
|
ENST00000630287.2:c.502A>G
|
ENSP00000486694.1:p.Ile168Val
|
|
NM_006516.2:c.502A>G
|
NP_006507.2:p.Ile168Val
|
|
NM_006516.3:c.502A>G
|
NP_006507.2:p.Ile168Val
|
|
NM_006516.4:c.502A>G
MANE Select
|
NP_006507.2:p.Ile168Val
|
|