ENST00000456935.7:c.2734A>G
MANE Select
|
ENSP00000395473.2:p.Met912Val
|
|
ENST00000221363.8:c.2731A>G
|
ENSP00000221363.4:p.Met911Val
|
|
ENST00000456935.6:c.2734A>G
|
ENSP00000395473.2:p.Met912Val
|
|
ENST00000466794.5:n.3324A>G
|
|
|
ENST00000469423.1:n.56A>G
|
|
|
ENST00000493218.5:n.145A>G
|
|
|
ENST00000597692.1:c.293A>G
|
|
|
NM_000528.3:c.2734A>G
|
NP_000519.2:p.Met912Val
|
|
NM_001173498.1:c.2731A>G
|
NP_001166969.1:p.Met911Val
|
|
XM_005259913.1:c.2737A>G
|
XP_005259970.1:p.Met913Val
|
|
XM_011528017.1:c.1633A>G
|
XP_011526319.1:p.Met545Val
|
|
XM_005259913.2:c.2737A>G
|
XP_005259970.1:p.Met913Val
|
|
XM_024451518.1:c.1633A>G
|
XP_024307286.1:p.Met545Val
|
|
NM_000528.4:c.2734A>G
MANE Select
|
NP_000519.2:p.Met912Val
|
|
NM_001173498.2:c.2731A>G
|
NP_001166969.1:p.Met911Val
|
|