ENST00000371270.6:c.1432T>G
MANE Select
|
ENSP00000360317.3:p.Ser478Ala
|
|
ENST00000371270.5:c.1432T>G
|
ENSP00000360317.3:p.Ser478Ala
|
|
ENST00000490994.6:c.*1218T>G
|
ENSP00000433314.1:n.*1218T>G
|
|
ENST00000525991.5:c.*1007T>G
|
ENSP00000433842.1:n.*1007T>G
|
|
ENST00000526814.5:n.1687T>G
|
|
|
ENST00000527420.5:c.*289T>G
|
ENSP00000433191.1:n.*289T>G
|
|
ENST00000527953.5:n.1726T>G
|
|
|
ENST00000533320.5:n.1666T>G
|
|
|
ENST00000535898.5:c.1126T>G
|
ENSP00000445062.1:p.Ser376Ala
|
|
ENST00000539050.5:c.1222T>G
|
ENSP00000442343.2:p.Ser408Ala
|
|
ENST00000623108.3:c.1222T>G
|
ENSP00000485110.1:p.Ser408Ala
|
|
NM_000770.3:c.1432T>G
MANE Select
|
NP_000761.3:p.Ser478Ala
|
|
NM_001198853.1:c.1222T>G
|
NP_001185782.1:p.Ser408Ala
|
|
NM_001198854.1:c.1126T>G
|
NP_001185783.1:p.Ser376Ala
|
|
NM_001198855.1:c.1222T>G
|
NP_001185784.1:p.Ser408Ala
|
|