ENST00000355832.10:c.3536A>T
MANE Select
|
ENSP00000348089.5:p.Tyr1179Phe
|
|
ENST00000679552.1:n.607A>T
|
|
|
ENST00000679871.1:n.682A>T
|
|
|
ENST00000679974.1:n.585A>T
|
|
|
ENST00000681632.1:n.4939A>T
|
|
|
ENST00000681659.1:c.3377A>T
|
ENSP00000505631.1:p.Tyr1126Phe
|
|
ENST00000355832.9:c.3536A>T
|
ENSP00000348089.5:p.Tyr1179Phe
|
|
ENST00000623073.3:c.*1832A>T
|
ENSP00000485650.1:n.*1832A>T
|
|
ENST00000623115.3:c.1646A>T
|
ENSP00000485321.1:p.Tyr549Phe
|
|
ENST00000624341.3:c.1368A>T
|
|
|
NM_000124.3:c.3536A>T
|
NP_000115.1:p.Tyr1179Phe
|
|
XR_945953.1:n.243-1141T>A
|
|
|
NM_001346440.1:c.3536A>T
|
NP_001333369.1:p.Tyr1179Phe
|
|
NM_000124.4:c.3536A>T
MANE Select
|
NP_000115.1:p.Tyr1179Phe
|
|
NM_001346440.2:c.3536A>T
|
NP_001333369.1:p.Tyr1179Phe
|
|