ENST00000324001.8:c.2092G>T
MANE Select
|
ENSP00000326018.6:p.Glu698Ter
|
|
ENST00000673881.1:c.1675G>T
|
ENSP00000501070.1:p.Glu559Ter
|
|
ENST00000674005.2:c.2377G>T
|
ENSP00000501261.1:p.Glu793Ter
|
|
ENST00000674773.1:c.1675G>T
|
ENSP00000502579.1:p.Glu559Ter
|
|
ENST00000675517.1:c.1967G>T
|
|
|
ENST00000676076.1:c.1953G>T
|
|
|
ENST00000676260.1:c.2054G>T
|
|
|
ENST00000676316.1:c.1979G>T
|
|
|
ENST00000291825.11:c.*2297G>T
|
ENSP00000291825.6:n.*2297G>T
|
|
ENST00000324001.7:c.2092G>T
|
ENSP00000326018.6:p.Glu698Ter
|
|
NM_020956.2:c.*2297G>T , LRG_265t1:c.*2297G>T
|
NP_066007.1:n.*2297G>T
|
|
NM_181882.2:c.2092G>T , LRG_265t2:c.2092G>T
|
NP_870998.2:p.Glu698Ter
|
|
XM_011527171.1:c.2092G>T
|
XP_011525473.1:p.Glu698Ter
|
|
XM_011527171.2:c.2092G>T
|
XP_011525473.1:p.Glu698Ter
|
|
XM_017027046.1:c.1990G>T
|
XP_016882535.1:p.Glu664Ter
|
|
XM_017027047.1:c.1990G>T
|
XP_016882536.1:p.Glu664Ter
|
|
NM_181882.3:c.2092G>T
MANE Select
|
NP_870998.2:p.Glu698Ter
|
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