ENST00000456935.7:c.1700C>A
MANE Select
|
ENSP00000395473.2:p.Ser567Ter
|
|
ENST00000221363.8:c.1697C>A
|
ENSP00000221363.4:p.Ser566Ter
|
|
ENST00000433513.5:n.306C>A
|
|
|
ENST00000456935.6:c.1700C>A
|
ENSP00000395473.2:p.Ser567Ter
|
|
ENST00000466794.5:n.2290C>A
|
|
|
ENST00000593686.1:c.293C>A
|
|
|
ENST00000595880.5:n.297C>A
|
|
|
ENST00000596591.1:c.64C>A
|
|
|
NM_000528.3:c.1700C>A
|
NP_000519.2:p.Ser567Ter
|
|
NM_001173498.1:c.1697C>A
|
NP_001166969.1:p.Ser566Ter
|
|
XM_005259913.1:c.1703C>A
|
XP_005259970.1:p.Ser568Ter
|
|
XM_011528017.1:c.599C>A
|
XP_011526319.1:p.Ser200Ter
|
|
XM_005259913.2:c.1703C>A
|
XP_005259970.1:p.Ser568Ter
|
|
XM_024451518.1:c.599C>A
|
XP_024307286.1:p.Ser200Ter
|
|
NM_000528.4:c.1700C>A
MANE Select
|
NP_000519.2:p.Ser567Ter
|
|
NM_001173498.2:c.1697C>A
|
NP_001166969.1:p.Ser566Ter
|
|