ENST00000695651.1:n.2660T>G
|
|
|
ENST00000695653.1:c.2221T>G
|
ENSP00000512084.1:p.Phe741Val
|
|
ENST00000695654.1:c.3337T>G
|
ENSP00000512085.1:p.Phe1113Val
|
|
ENST00000695689.1:c.283T>G
|
ENSP00000512101.1:n.283T>G
|
|
ENST00000695690.1:n.503T>G
|
|
|
ENST00000695691.1:n.503T>G
|
|
|
ENST00000245907.11:c.4312T>G
MANE Select
|
ENSP00000245907.4:p.Phe1438Val
|
|
ENST00000245907.10:c.4312T>G
|
ENSP00000245907.4:p.Phe1438Val
|
|
ENST00000596548.1:c.433T>G
|
ENSP00000469744.1:p.Phe145Val
|
|
ENST00000599899.5:n.1271T>G
|
|
|
ENST00000601008.1:c.242-4021T>G
|
ENSP00000471384.1:n.242-4021T>G
|
|
NM_000064.3:c.4312T>G
|
NP_000055.2:p.Phe1438Val
|
|
NM_000064.4:c.4312T>G
MANE Select
|
NP_000055.2:p.Phe1438Val
|
|