ENST00000302347.10:c.1246C>T
|
ENSP00000303242.6:p.His416Tyr
|
|
ENST00000652462.1:c.1174C>T
MANE Select
|
ENSP00000498780.1:p.His392Tyr
|
|
ENST00000302347.9:c.1174C>T
|
ENSP00000303242.5:p.His392Tyr
|
|
ENST00000355153.8:c.1174C>T
|
ENSP00000347279.4:p.His392Tyr
|
|
ENST00000397850.6:c.1174C>T
|
ENSP00000380948.2:p.His392Tyr
|
|
ENST00000397852.5:c.1174C>T
|
ENSP00000380950.1:p.His392Tyr
|
|
ENST00000397854.7:c.1003C>T
|
ENSP00000380952.3:p.His335Tyr
|
|
ENST00000397857.5:c.1174C>T
|
ENSP00000380955.1:p.His392Tyr
|
|
ENST00000475170.5:n.574C>T
|
|
|
ENST00000498666.5:n.2743C>T
|
|
|
ENST00000523323.5:c.*1001C>T
|
ENSP00000427732.1:n.*1001C>T
|
|
ENST00000610622.4:c.1003C>T
|
ENSP00000480700.1:p.His335Tyr
|
|
NM_000211.4:c.1174C>T
|
NP_000202.3:p.His392Tyr
|
|
NM_001127491.2:c.1174C>T
|
NP_001120963.2:p.His392Tyr
|
|
NM_001303238.1:c.967C>T
|
NP_001290167.1:p.His323Tyr
|
|
XM_006724001.1:c.967C>T
|
XP_006724064.1:p.His323Tyr
|
|
XM_006724001.2:c.967C>T
|
XP_006724064.1:p.His323Tyr
|
|
NM_000211.5:c.1174C>T
MANE Select
|
NP_000202.3:p.His392Tyr
|
|
NM_001127491.3:c.1174C>T
|
NP_001120963.2:p.His392Tyr
|
|
NM_001303238.2:c.967C>T
|
NP_001290167.1:p.His323Tyr
|
|