ENST00000225573.5:c.657A>T
|
ENSP00000225573.5:p.Ter219Tyr
|
|
ENST00000434554.7:c.732A>T
|
ENSP00000399960.3:p.Ter244Tyr
|
|
ENST00000582171.6:c.*451A>T
|
ENSP00000463994.1:n.*451A>T
|
|
ENST00000584061.6:c.717A>T
|
ENSP00000463972.2:p.Ter239Tyr
|
|
ENST00000584806.2:n.455A>T
|
|
|
ENST00000641305.1:n.2285A>T
|
|
|
ENST00000641323.1:c.*805A>T
|
ENSP00000492965.1:n.*805A>T
|
|
ENST00000641427.1:n.786A>T
|
|
|
ENST00000641703.1:c.502A>T
|
ENSP00000493219.1:n.502A>T
|
|
ENST00000641709.1:c.*608A>T
|
ENSP00000493349.1:n.*608A>T
|
|
ENST00000641856.1:c.*1294A>T
|
ENSP00000493224.1:n.*1294A>T
|
|
ENST00000642017.2:c.786A>T
MANE Select
|
ENSP00000493302.2:p.Ter262Tyr
|
|
ENST00000225573.4:c.786A>T
|
ENSP00000225573.4:p.Ter262Tyr
|
|
ENST00000434554.6:c.657A>T
|
ENSP00000399960.2:p.Ter219Tyr
|
|
ENST00000582171.5:c.*451A>T
|
ENSP00000463994.1:n.*451A>T
|
|
ENST00000584806.1:n.455A>T
|
|
|
NM_018129.3:c.786A>T
|
NP_060599.1:p.Ter262Tyr
|
|
XM_005257500.2:c.546A>T
|
XP_005257557.1:p.Ter182Tyr
|
|
XM_011524968.1:c.501A>T
|
XP_011523270.1:p.Ter167Tyr
|
|
XM_005257500.3:c.546A>T
|
XP_005257557.1:p.Ter182Tyr
|
|
XM_011524968.2:c.501A>T
|
XP_011523270.1:p.Ter167Tyr
|
|
XM_017024813.1:c.546A>T
|
XP_016880302.1:p.Ter182Tyr
|
|
NM_018129.4:c.786A>T
MANE Select
|
NP_060599.1:p.Ter262Tyr
|
|