ENST00000405440.7:c.229A>T
MANE Select
|
ENSP00000384152.3:p.Thr77Ser
|
|
ENST00000310346.8:c.229A>T
|
ENSP00000309913.4:p.Thr77Ser
|
|
ENST00000349716.9:c.79A>T
|
ENSP00000337723.5:p.Thr27Ser
|
|
ENST00000405440.6:c.229A>T
|
ENSP00000384152.2:p.Thr77Ser
|
|
ENST00000526441.1:c.229A>T
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ENSP00000433292.1:p.Thr77Ser
|
|
ENST00000552726.1:n.280A>T
|
|
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NM_000192.3:c.229A>T , LRG_670t1:c.229A>T
|
NP_000183.2:p.Thr77Ser
|
|
NM_080717.2:c.79A>T
|
NP_542448.1:p.Thr27Ser
|
|
NM_181486.2:c.229A>T
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NP_852259.1:p.Thr77Ser
|
|
XM_017019912.1:c.277A>T
|
XP_016875401.1:p.Thr93Ser
|
|
NM_080717.3:c.79A>T
|
NP_542448.1:p.Thr27Ser
|
|
NM_181486.4:c.229A>T
MANE Select
|
NP_852259.1:p.Thr77Ser
|
|
NM_080717.4:c.79A>T
|
NP_542448.1:p.Thr27Ser
|
|