ENST00000324001.8:c.3338A>T
MANE Select
|
ENSP00000326018.6:p.Glu1113Val
|
|
ENST00000673881.1:c.2921A>T
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ENSP00000501070.1:p.Glu974Val
|
|
ENST00000674005.2:c.3623A>T
|
ENSP00000501261.1:p.Glu1208Val
|
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ENST00000674773.1:c.2921A>T
|
ENSP00000502579.1:p.Glu974Val
|
|
ENST00000675517.1:c.3213A>T
|
|
|
ENST00000676076.1:c.3199A>T
|
|
|
ENST00000676260.1:c.3300A>T
|
|
|
ENST00000676316.1:c.3225A>T
|
|
|
ENST00000291825.11:c.*3543A>T
|
ENSP00000291825.6:n.*3543A>T
|
|
ENST00000324001.7:c.3338A>T
|
ENSP00000326018.6:p.Glu1113Val
|
|
NM_020956.2:c.*3543A>T , LRG_265t1:c.*3543A>T
|
NP_066007.1:n.*3543A>T
|
|
NM_181882.2:c.3338A>T , LRG_265t2:c.3338A>T
|
NP_870998.2:p.Glu1113Val
|
|
XM_011527171.1:c.3338A>T
|
XP_011525473.1:p.Glu1113Val
|
|
XM_011527171.2:c.3338A>T
|
XP_011525473.1:p.Glu1113Val
|
|
XM_017027046.1:c.3236A>T
|
XP_016882535.1:p.Glu1079Val
|
|
XM_017027047.1:c.3236A>T
|
XP_016882536.1:p.Glu1079Val
|
|
NM_181882.3:c.3338A>T
MANE Select
|
NP_870998.2:p.Glu1113Val
|
|