ENST00000639857.2:c.1558C>T
|
ENSP00000491593.2:p.His520Tyr
|
|
ENST00000685487.1:c.1558C>T
|
ENSP00000508503.1:p.His520Tyr
|
|
ENST00000687624.1:n.223C>T
|
|
|
ENST00000687906.1:c.1444C>T
|
ENSP00000509536.1:p.His482Tyr
|
|
ENST00000688597.1:c.1224+6929C>T
|
ENSP00000510628.1:n.1224+6929C>T
|
|
ENST00000688701.1:n.802C>T
|
|
|
ENST00000690210.1:c.1558C>T
|
ENSP00000509272.1:p.His520Tyr
|
|
ENST00000690472.1:n.767C>T
|
|
|
ENST00000692624.1:c.*104C>T
|
ENSP00000508953.1:n.*104C>T
|
|
ENST00000351677.7:c.1558C>T
MANE Select
|
ENSP00000340944.3:p.His520Tyr
|
|
ENST00000351677.6:c.1558C>T
|
ENSP00000340944.2:p.His520Tyr
|
|
ENST00000635625.1:c.1570C>T
|
ENSP00000489597.1:p.His524Tyr
|
|
ENST00000635652.1:c.571C>T
|
ENSP00000489541.1:p.His191Tyr
|
|
NM_002834.3:c.1558C>T , LRG_614t1:c.1558C>T
|
NP_002825.3:p.His520Tyr
|
|
XM_006719526.1:c.1570C>T
|
XP_006719589.1:p.His524Tyr
|
|
XM_006719527.1:c.1456C>T
|
XP_006719590.1:p.His486Tyr
|
|
XM_011538613.1:c.1567C>T
|
XP_011536915.1:p.His523Tyr
|
|
NM_001330437.1:c.1570C>T
|
NP_001317366.1:p.His524Tyr
|
|
NM_002834.4:c.1558C>T
|
NP_002825.3:p.His520Tyr
|
|
XM_011538613.2:c.1567C>T
|
XP_011536915.1:p.His523Tyr
|
|
XM_017019722.1:c.1555C>T
|
XP_016875211.1:p.His519Tyr
|
|
NM_001330437.2:c.1570C>T
|
NP_001317366.1:p.His524Tyr
|
|
NM_001374625.1:c.1555C>T
|
NP_001361554.1:p.His519Tyr
|
|
NM_002834.5:c.1558C>T
MANE Select
|
NP_002825.3:p.His520Tyr
|
|