ENST00000524470.2:c.*1090A>C
|
ENSP00000514307.1:n.*1090A>C
|
|
ENST00000525976.6:c.2741A>C
|
ENSP00000434831.2:p.Tyr914Ser
|
|
ENST00000527481.3:c.2741A>C
|
ENSP00000466340.2:p.Tyr914Ser
|
|
ENST00000529370.6:n.4117A>C
|
|
|
ENST00000529739.2:n.3155A>C
|
|
|
ENST00000530829.2:c.*2292A>C
|
ENSP00000436826.2:n.*2292A>C
|
|
ENST00000531836.6:c.2741A>C
|
ENSP00000436175.2:p.Tyr914Ser
|
|
ENST00000533334.2:c.*783A>C
|
ENSP00000432320.2:n.*783A>C
|
|
ENST00000534228.2:n.4200A>C
|
|
|
ENST00000699354.1:n.843A>C
|
|
|
ENST00000699355.1:c.*1846A>C
|
ENSP00000514328.1:n.*1846A>C
|
|
ENST00000699356.1:n.3155A>C
|
|
|
ENST00000699357.1:n.4200A>C
|
|
|
ENST00000699358.1:c.2741A>C
|
ENSP00000514329.1:p.Tyr914Ser
|
|
ENST00000699360.1:c.2741A>C
|
ENSP00000514331.1:p.Tyr914Ser
|
|
ENST00000525621.6:c.2741A>C
MANE Select
|
ENSP00000431885.1:p.Tyr914Ser
|
|
ENST00000264818.10:c.2741A>C
|
ENSP00000264818.6:p.Tyr914Ser
|
|
ENST00000524462.5:c.2186A>C
|
ENSP00000433203.1:p.Tyr729Ser
|
|
ENST00000525621.5:c.2741A>C
|
ENSP00000431885.1:p.Tyr914Ser
|
|
ENST00000527481.2:c.37A>C
|
|
|
ENST00000529412.1:n.413A>C
|
|
|
ENST00000530560.5:c.170A>C
|
ENSP00000465291.1:p.Tyr57Ser
|
|
NM_003331.4:c.2741A>C , LRG_121t1:c.2741A>C
|
NP_003322.3:p.Tyr914Ser
|
|
XM_011528245.1:c.2741A>C
|
XP_011526547.1:p.Tyr914Ser
|
|
XM_011528246.1:c.2444A>C
|
XP_011526548.1:p.Tyr815Ser
|
|
XM_011528247.1:c.2444A>C
|
XP_011526549.1:p.Tyr815Ser
|
|
XM_011528248.1:c.2741A>C
|
XP_011526550.1:p.Tyr914Ser
|
|
XM_011528249.1:c.1415A>C
|
XP_011526551.1:p.Tyr472Ser
|
|
XM_011528251.1:c.998A>C
|
XP_011526553.1:p.Tyr333Ser
|
|
XM_011528246.3:c.2444A>C
|
XP_011526548.1:p.Tyr815Ser
|
|
XM_011528249.2:c.1415A>C
|
XP_011526551.1:p.Tyr472Ser
|
|
XR_001753750.1:n.2898A>C
|
|
|
XR_001753751.1:n.2898A>C
|
|
|
XR_002958353.1:n.3824A>C
|
|
|
NM_003331.5:c.2741A>C
MANE Select
|
NP_003322.3:p.Tyr914Ser
|
|
NM_001385197.1:c.2741A>C
|
NP_001372126.1:p.Tyr914Ser
|
|
NM_001385198.1:c.2741A>C
|
NP_001372127.1:p.Tyr914Ser
|
|
NM_001385199.1:c.2555A>C
|
NP_001372128.1:p.Tyr852Ser
|
|
NM_001385200.1:c.2738A>C
|
NP_001372129.1:p.Tyr913Ser
|
|
NM_001385201.1:c.2543A>C
|
NP_001372130.1:p.Tyr848Ser
|
|
NM_001385202.1:c.2657A>C
|
NP_001372131.1:p.Tyr886Ser
|
|
NM_001385203.1:c.2822A>C
|
NP_001372132.1:p.Tyr941Ser
|
|
NM_001385204.1:c.2951A>C
|
NP_001372133.1:p.Tyr984Ser
|
|
NM_001385205.1:c.2651A>C
|
NP_001372134.1:p.Tyr884Ser
|
|
NM_001385206.1:c.2615A>C
|
NP_001372135.1:p.Tyr872Ser
|
|
NM_001385207.1:c.2723A>C
|
NP_001372136.1:p.Tyr908Ser
|
|