ENST00000309383.6:c.2125A>G
MANE Select
|
ENSP00000310649.1:p.Ile709Val
|
|
ENST00000309383.5:c.2125A>G
|
ENSP00000310649.1:p.Ile709Val
|
|
ENST00000326848.7:c.1210A>G
|
ENSP00000320853.7:p.Ile404Val
|
|
ENST00000590333.5:c.2173A>G
|
ENSP00000468190.1:p.Ile725Val
|
|
NM_032430.1:c.2125A>G
|
NP_115806.1:p.Ile709Val
|
|
XM_005259327.2:c.1855A>G
|
XP_005259384.1:p.Ile619Val
|
|
XM_011527395.1:c.1882A>G
|
XP_011525697.1:p.Ile628Val
|
|
XR_430213.2:n.2108A>G
|
|
|
XM_005259327.3:c.1855A>G
|
XP_005259384.1:p.Ile619Val
|
|
XM_011527395.2:c.1597A>G
|
XP_011525697.2:p.Ile533Val
|
|
XM_024451739.1:c.1900A>G
|
XP_024307507.1:p.Ile634Val
|
|
XR_430213.4:n.2406A>G
|
|
|
NM_032430.2:c.2125A>G
MANE Select
|
NP_115806.1:p.Ile709Val
|
|