ENST00000309383.6:c.2095A>T
MANE Select
|
ENSP00000310649.1:p.Ser699Cys
|
|
ENST00000309383.5:c.2095A>T
|
ENSP00000310649.1:p.Ser699Cys
|
|
ENST00000326848.7:c.1180A>T
|
ENSP00000320853.7:p.Ser394Cys
|
|
ENST00000590333.5:c.2143A>T
|
ENSP00000468190.1:p.Ser715Cys
|
|
NM_032430.1:c.2095A>T
|
NP_115806.1:p.Ser699Cys
|
|
XM_005259327.2:c.1825A>T
|
XP_005259384.1:p.Ser609Cys
|
|
XM_011527395.1:c.1852A>T
|
XP_011525697.1:p.Ser618Cys
|
|
XR_430213.2:n.2078A>T
|
|
|
XM_005259327.3:c.1825A>T
|
XP_005259384.1:p.Ser609Cys
|
|
XM_011527395.2:c.1567A>T
|
XP_011525697.2:p.Ser523Cys
|
|
XM_024451739.1:c.1870A>T
|
XP_024307507.1:p.Ser624Cys
|
|
XR_430213.4:n.2376A>T
|
|
|
NM_032430.2:c.2095A>T
MANE Select
|
NP_115806.1:p.Ser699Cys
|
|