|
ENST00000689298.1:c.*2178C>T
|
ENSP00000508434.1:n.*2178C>T
|
|
|
ENST00000440875.6:c.1552C>T
|
ENSP00000475553.3:p.His518Tyr
|
|
|
ENST00000627532.3:c.2329C>T
MANE Select
|
ENSP00000487174.1:p.His777Tyr
|
|
|
ENST00000636026.2:c.2329C>T
|
ENSP00000490776.1:p.His777Tyr
|
|
|
ENST00000636179.1:n.2298C>T
|
|
|
|
ENST00000636413.1:c.1993C>T
|
ENSP00000490508.1:p.His665Tyr
|
|
|
ENST00000636471.1:c.2404C>T
|
ENSP00000490317.1:p.His802Tyr
|
|
|
ENST00000636732.2:c.*2046C>T
|
ENSP00000490175.1:n.*2046C>T
|
|
|
ENST00000636820.1:n.2429C>T
|
|
|
|
ENST00000637045.1:c.1993C>T
|
ENSP00000490141.1:p.His665Tyr
|
|
|
ENST00000637304.1:c.1993C>T
|
ENSP00000490872.1:p.His665Tyr
|
|
|
ENST00000638007.1:c.1993C>T
|
ENSP00000490723.1:p.His665Tyr
|
|
|
ENST00000638087.1:c.1993C>T
|
ENSP00000490673.1:p.His665Tyr
|
|
|
ENST00000638128.1:c.1552C>T
|
ENSP00000490934.1:p.His518Tyr
|
|
|
ENST00000675069.1:c.-133-8C>T
|
ENSP00000502467.1:n.-133-8C>T
|
|
|
ENST00000675145.1:n.2877C>T
|
|
|
|
ENST00000303660.8:c.2326C>T
|
ENSP00000302501.4:p.His776Tyr
|
|
|
ENST00000409487.7:c.2329C>T
|
ENSP00000386854.2:p.His777Tyr
|
|
|
ENST00000419938.5:c.655+2341C>T
|
ENSP00000394777.2:n.655+2341C>T
|
|
|
ENST00000440875.5:c.1167+679C>T
|
ENSP00000475553.2:n.1167+679C>T
|
|
|
ENST00000539609.7:c.2257C>T
|
ENSP00000443792.2:p.His753Tyr
|
|
|
ENST00000558170.6:c.2329C>T
|
ENSP00000454157.1:p.His777Tyr
|
|
|
ENST00000627532.2:c.2329C>T
|
ENSP00000487174.1:p.His777Tyr
|
|
|
NM_001171653.1:c.2257C>T
|
NP_001165124.1:p.His753Tyr
|
|
|
NM_014795.3:c.2329C>T
|
NP_055610.1:p.His777Tyr
|
|
|
XM_006712881.2:c.2329C>T
|
XP_006712944.1:p.His777Tyr
|
|
|
XM_006712882.2:c.2329C>T
|
XP_006712945.1:p.His777Tyr
|
|
|
XM_011512231.1:c.2320C>T
|
XP_011510533.1:p.His774Tyr
|
|
|
XM_011512232.1:c.2308C>T
|
XP_011510534.1:p.His770Tyr
|
|
|
NM_014795.4:c.2329C>T
MANE Select
|
NP_055610.1:p.His777Tyr
|
|
|
NM_001171653.2:c.2257C>T
|
NP_001165124.1:p.His753Tyr
|
|
