ENST00000553509.2:c.1478A>T
|
ENSP00000450989.2:p.Tyr493Phe
|
|
ENST00000556478.3:c.1478A>T
|
ENSP00000501428.2:p.Tyr493Phe
|
|
ENST00000682037.1:c.1478A>T
|
ENSP00000508289.1:p.Tyr493Phe
|
|
ENST00000682219.1:n.2816A>T
|
|
|
ENST00000683037.1:n.1399A>T
|
|
|
ENST00000683330.1:n.1812A>T
|
|
|
ENST00000358385.12:c.1478A>T
MANE Select
|
ENSP00000351155.7:p.Tyr493Phe
|
|
ENST00000674288.1:c.*2770A>T
|
ENSP00000501522.1:n.*2770A>T
|
|
ENST00000358385.10:c.1478A>T
|
ENSP00000351155.6:p.Tyr493Phe
|
|
ENST00000441560.6:c.1478A>T
|
ENSP00000413675.2:p.Tyr493Phe
|
|
ENST00000556067.1:c.224A>T
|
ENSP00000451100.1:p.Tyr75Phe
|
|
NM_001127713.1:c.1478A>T
|
NP_001121185.1:p.Tyr493Phe
|
|
NM_015915.4:c.1478A>T
|
NP_056999.2:p.Tyr493Phe
|
|
NM_181598.3:c.1478A>T
|
NP_853629.2:p.Tyr493Phe
|
|
NM_015915.5:c.1478A>T
MANE Select
|
NP_056999.2:p.Tyr493Phe
|
|
NM_181598.4:c.1478A>T
|
NP_853629.2:p.Tyr493Phe
|
|