ENST00000309383.6:c.2179G>T
MANE Select
|
ENSP00000310649.1:p.Asp727Tyr
|
|
ENST00000309383.5:c.2179G>T
|
ENSP00000310649.1:p.Asp727Tyr
|
|
ENST00000326848.7:c.1264G>T
|
ENSP00000320853.7:p.Asp422Tyr
|
|
ENST00000590333.5:c.2227G>T
|
ENSP00000468190.1:p.Asp743Tyr
|
|
NM_032430.1:c.2179G>T
|
NP_115806.1:p.Asp727Tyr
|
|
XM_005259327.2:c.1909G>T
|
XP_005259384.1:p.Asp637Tyr
|
|
XM_011527395.1:c.1936G>T
|
XP_011525697.1:p.Asp646Tyr
|
|
XR_430213.2:n.2162G>T
|
|
|
XM_005259327.3:c.1909G>T
|
XP_005259384.1:p.Asp637Tyr
|
|
XM_011527395.2:c.1651G>T
|
XP_011525697.2:p.Asp551Tyr
|
|
XM_024451739.1:c.1954G>T
|
XP_024307507.1:p.Asp652Tyr
|
|
XR_430213.4:n.2460G>T
|
|
|
NM_032430.2:c.2179G>T
MANE Select
|
NP_115806.1:p.Asp727Tyr
|
|