ENST00000309383.6:c.2158C>G
MANE Select
|
ENSP00000310649.1:p.Pro720Ala
|
|
ENST00000309383.5:c.2158C>G
|
ENSP00000310649.1:p.Pro720Ala
|
|
ENST00000326848.7:c.1243C>G
|
ENSP00000320853.7:p.Pro415Ala
|
|
ENST00000590333.5:c.2206C>G
|
ENSP00000468190.1:p.Pro736Ala
|
|
NM_032430.1:c.2158C>G
|
NP_115806.1:p.Pro720Ala
|
|
XM_005259327.2:c.1888C>G
|
XP_005259384.1:p.Pro630Ala
|
|
XM_011527395.1:c.1915C>G
|
XP_011525697.1:p.Pro639Ala
|
|
XR_430213.2:n.2141C>G
|
|
|
XM_005259327.3:c.1888C>G
|
XP_005259384.1:p.Pro630Ala
|
|
XM_011527395.2:c.1630C>G
|
XP_011525697.2:p.Pro544Ala
|
|
XM_024451739.1:c.1933C>G
|
XP_024307507.1:p.Pro645Ala
|
|
XR_430213.4:n.2439C>G
|
|
|
NM_032430.2:c.2158C>G
MANE Select
|
NP_115806.1:p.Pro720Ala
|
|