ENST00000357578.8:c.1258T>C
MANE Select
|
ENSP00000350191.3:p.Phe420Leu
|
|
ENST00000479394.2:n.373T>C
|
|
|
ENST00000672352.1:c.877T>C
|
ENSP00000500876.1:p.Phe293Leu
|
|
ENST00000672652.1:c.1221T>C
|
|
|
ENST00000348925.2:c.1297T>C
|
ENSP00000314649.3:p.Phe433Leu
|
|
ENST00000357578.7:c.1258T>C
|
ENSP00000350191.3:p.Phe420Leu
|
|
ENST00000479394.1:n.373T>C
|
|
|
ENST00000491546.5:c.1174T>C
|
ENSP00000417687.1:p.Phe392Leu
|
|
NM_001080.3:c.1258T>C
MANE Select
|
NP_001071.1:p.Phe420Leu
|
|
NM_170740.1:c.1297T>C
|
NP_733936.1:p.Phe433Leu
|
|
NM_001368954.1:c.1114T>C
|
NP_001355883.1:p.Phe372Leu
|
|