ENST00000327047.6:c.348A>T
MANE Select
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ENSP00000322280.1:p.Thr116=
|
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ENST00000468836.2:c.496A>T
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ENSP00000419892.2:p.Ser166Cys
|
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ENST00000644099.1:c.340A>T
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ENSP00000494762.1:n.340A>T
|
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ENST00000295911.6:c.120A>T
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ENSP00000295911.2:p.Thr40=
|
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ENST00000327047.5:c.348A>T
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ENSP00000322280.1:p.Thr116=
|
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ENST00000328863.8:c.348A>T
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ENSP00000329158.4:p.Thr116=
|
|
ENST00000468836.1:c.120A>T
|
ENSP00000419892.1:p.Thr40=
|
|
ENST00000472224.1:n.354A>T
|
|
|
ENST00000485607.1:c.12A>T
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ENSP00000419244.1:p.Thr4=
|
|
ENST00000562308.5:c.19A>T
|
|
|
ENST00000565169.1:c.77A>T
|
|
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ENST00000569170.5:c.77A>T
|
|
|
NM_001195794.1:c.348A>T , LRG_700t1:c.348A>T
|
NP_001182723.1:p.Thr116=
|
|
NM_001256819.1:c.520A>T
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NP_001243748.1:p.Ser174Cys
|
|
NM_052995.2:c.120A>T , LRG_700t2:c.120A>T
|
NP_443721.1:p.Thr40=
|
|
NM_174878.2:c.348A>T
|
NP_777367.1:p.Thr116=
|
|
NR_046380.2:n.790A>T
|
|
|
XR_924167.1:n.660A>T
|
|
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NM_001256819.2:c.520A>T
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NP_001243748.1:p.Ser174Cys
|
|
NM_174878.3:c.348A>T
MANE Select
|
NP_777367.1:p.Thr116=
|
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NR_046380.3:n.518A>T
|
|
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