ENST00000218224.9:c.706G>A
|
ENSP00000218224.4:p.Ala236Thr
|
|
ENST00000376563.6:c.706G>A
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ENSP00000365747.1:p.Ala236Thr
|
|
ENST00000396763.6:c.706G>A
|
ENSP00000379985.1:p.Ala236Thr
|
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ENST00000443648.6:c.706G>A
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ENSP00000414861.2:p.Ala236Thr
|
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ENST00000456306.2:c.97G>A
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ENSP00000393013.2:p.Ala33Thr
|
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ENST00000472742.6:c.*123G>A
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ENSP00000509191.1:n.*123G>A
|
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ENST00000474671.6:n.1861G>A
|
|
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ENST00000477997.6:n.1655G>A
|
|
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ENST00000486150.6:n.1961G>A
|
|
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ENST00000692023.1:c.*1127G>A
|
ENSP00000509927.1:n.*1127G>A
|
|
ENST00000447146.7:c.706G>A
MANE Select
|
ENSP00000391759.2:p.Ala236Thr
|
|
ENST00000651767.1:c.706G>A
|
ENSP00000498362.1:p.Ala236Thr
|
|
ENST00000218224.8:c.706G>A
|
ENSP00000218224.4:p.Ala236Thr
|
|
ENST00000247140.8:c.421G>A
|
ENSP00000247140.4:p.Ala141Thr
|
|
ENST00000376563.5:c.706G>A
|
ENSP00000365747.1:p.Ala236Thr
|
|
ENST00000376566.8:c.421G>A
|
ENSP00000365750.4:p.Ala141Thr
|
|
ENST00000396763.5:c.706G>A
|
ENSP00000379985.1:p.Ala236Thr
|
|
ENST00000447146.6:c.706G>A
|
ENSP00000391759.2:p.Ala236Thr
|
|
ENST00000456306.1:c.387G>A
|
|
|
ENST00000463529.4:n.1052G>A
|
|
|
ENST00000465859.2:n.720G>A
|
|
|
ENST00000470059.5:n.920G>A
|
|
|
ENST00000470062.5:n.678G>A
|
|
|
ENST00000473764.5:n.1278G>A
|
|
|
ENST00000474671.5:n.766G>A
|
|
|
ENST00000477997.5:n.787G>A
|
|
|
NM_001032381.1:c.706G>A
|
NP_001027553.1:p.Ala236Thr
|
|
NM_001032382.1:c.706G>A
|
NP_001027554.1:p.Ala236Thr
|
|
NM_001032383.1:c.706G>A
|
NP_001027555.1:p.Ala236Thr
|
|
NM_001032384.1:c.706G>A
|
NP_001027556.1:p.Ala236Thr
|
|
NM_001167989.1:c.703G>A
|
NP_001161461.1:p.Ala235Thr
|
|
NM_001167990.1:c.682G>A
|
NP_001161462.1:p.Ala228Thr
|
|
NM_001167992.1:c.406G>A
|
NP_001161464.1:p.Ala136Thr
|
|
NM_005710.2:c.706G>A
|
NP_005701.1:p.Ala236Thr
|
|
NM_144495.2:c.421G>A
|
NP_652766.1:p.Ala141Thr
|
|
XM_005272571.3:c.703G>A
|
XP_005272628.1:p.Ala235Thr
|
|
XM_005272572.3:c.421G>A
|
XP_005272629.1:p.Ala141Thr
|
|
XM_011543884.1:c.706G>A
|
XP_011542186.1:p.Ala236Thr
|
|
XM_005272572.4:c.421G>A
|
XP_005272629.1:p.Ala141Thr
|
|
XM_011543884.2:c.706G>A
|
XP_011542186.1:p.Ala236Thr
|
|
XM_017029207.1:c.703G>A
|
XP_016884696.1:p.Ala235Thr
|
|
NM_001032381.2:c.706G>A
|
NP_001027553.1:p.Ala236Thr
|
|
NM_001032382.2:c.706G>A
MANE Select
|
NP_001027554.1:p.Ala236Thr
|
|
NM_001032383.2:c.706G>A
|
NP_001027555.1:p.Ala236Thr
|
|
NM_001167989.2:c.703G>A
|
NP_001161461.1:p.Ala235Thr
|
|
NM_001167990.2:c.682G>A
|
NP_001161462.1:p.Ala228Thr
|
|
NM_144495.3:c.421G>A
|
NP_652766.1:p.Ala141Thr
|
|