ENST00000371270.6:c.1461C>G
MANE Select
|
ENSP00000360317.3:p.Phe487Leu
|
|
ENST00000371270.5:c.1461C>G
|
ENSP00000360317.3:p.Phe487Leu
|
|
ENST00000490994.6:c.*1247C>G
|
ENSP00000433314.1:n.*1247C>G
|
|
ENST00000525991.5:c.*1036C>G
|
ENSP00000433842.1:n.*1036C>G
|
|
ENST00000526814.5:n.1716C>G
|
|
|
ENST00000527420.5:c.*318C>G
|
ENSP00000433191.1:n.*318C>G
|
|
ENST00000527953.5:n.1755C>G
|
|
|
ENST00000533320.5:n.1695C>G
|
|
|
ENST00000535898.5:c.1155C>G
|
ENSP00000445062.1:p.Phe385Leu
|
|
ENST00000539050.5:c.1251C>G
|
ENSP00000442343.2:p.Phe417Leu
|
|
ENST00000623108.3:c.1251C>G
|
ENSP00000485110.1:p.Phe417Leu
|
|
NM_000770.3:c.1461C>G
MANE Select
|
NP_000761.3:p.Phe487Leu
|
|
NM_001198853.1:c.1251C>G
|
NP_001185782.1:p.Phe417Leu
|
|
NM_001198854.1:c.1155C>G
|
NP_001185783.1:p.Phe385Leu
|
|
NM_001198855.1:c.1251C>G
|
NP_001185784.1:p.Phe417Leu
|
|