ENST00000309383.6:c.2132C>A
MANE Select
|
ENSP00000310649.1:p.Ala711Glu
|
|
ENST00000309383.5:c.2132C>A
|
ENSP00000310649.1:p.Ala711Glu
|
|
ENST00000326848.7:c.1217C>A
|
ENSP00000320853.7:p.Ala406Glu
|
|
ENST00000590333.5:c.2180C>A
|
ENSP00000468190.1:p.Ala727Glu
|
|
NM_032430.1:c.2132C>A
|
NP_115806.1:p.Ala711Glu
|
|
XM_005259327.2:c.1862C>A
|
XP_005259384.1:p.Ala621Glu
|
|
XM_011527395.1:c.1889C>A
|
XP_011525697.1:p.Ala630Glu
|
|
XR_430213.2:n.2115C>A
|
|
|
XM_005259327.3:c.1862C>A
|
XP_005259384.1:p.Ala621Glu
|
|
XM_011527395.2:c.1604C>A
|
XP_011525697.2:p.Ala535Glu
|
|
XM_024451739.1:c.1907C>A
|
XP_024307507.1:p.Ala636Glu
|
|
XR_430213.4:n.2413C>A
|
|
|
NM_032430.2:c.2132C>A
MANE Select
|
NP_115806.1:p.Ala711Glu
|
|