ENST00000307998.11:c.908T>C
MANE Select
|
ENSP00000309953.6:p.Phe303Ser
|
|
ENST00000307998.10:c.908T>C
|
ENSP00000309953.6:p.Phe303Ser
|
|
ENST00000525392.1:n.69T>C
|
|
|
ENST00000526628.5:n.1474T>C
|
|
|
ENST00000528176.5:c.908T>C
|
ENSP00000434151.1:p.Phe303Ser
|
|
ENST00000528409.1:n.152T>C
|
|
|
ENST00000530806.5:c.-91T>C
|
ENSP00000436526.1:n.-91T>C
|
|
ENST00000531005.5:n.1902T>C
|
|
|
ENST00000531645.5:c.56T>C
|
ENSP00000436521.1:p.Phe19Ser
|
|
ENST00000531972.5:c.908T>C
|
ENSP00000435295.1:p.Phe303Ser
|
|
ENST00000532084.5:n.334T>C
|
|
|
NM_016938.4:c.908T>C
|
NP_058634.4:p.Phe303Ser
|
|
NR_037718.1:n.1167T>C
|
|
|
NM_016938.5:c.908T>C
MANE Select
|
NP_058634.4:p.Phe303Ser
|
|
NR_037718.2:n.1033T>C
|
|
|