ENST00000388913.4:c.874G>A
MANE Select
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ENSP00000373565.3:p.Ala292Thr
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ENST00000650760.1:c.1477G>A
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ENSP00000499217.1:p.Ala493Thr
|
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ENST00000388913.3:c.874G>A
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ENSP00000373565.3:p.Ala292Thr
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ENST00000395103.2:c.54G>A
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|
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NM_198488.3:c.874G>A
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NP_940890.3:p.Ala292Thr
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XM_005250887.2:c.931G>A
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XP_005250944.1:p.Ala311Thr
|
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XM_005250888.2:c.892G>A
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XP_005250945.1:p.Ala298Thr
|
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XM_005250889.2:c.874G>A
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XP_005250946.1:p.Ala292Thr
|
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XM_011516980.1:c.1195G>A
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XP_011515282.1:p.Ala399Thr
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XM_011516981.1:c.1042G>A
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XP_011515283.1:p.Ala348Thr
|
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XM_005250887.3:c.931G>A
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XP_005250944.1:p.Ala311Thr
|
|
XM_005250888.3:c.892G>A
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XP_005250945.1:p.Ala298Thr
|
|
XM_005250889.3:c.874G>A
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XP_005250946.1:p.Ala292Thr
|
|
XM_011516980.2:c.1477G>A
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XP_011515282.2:p.Ala493Thr
|
|
XM_011516981.2:c.1042G>A
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XP_011515283.1:p.Ala348Thr
|
|
XM_024447131.1:c.874G>A
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XP_024302899.1:p.Ala292Thr
|
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NM_198488.4:c.874G>A
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NP_940890.3:p.Ala292Thr
|
|
NM_198488.5:c.874G>A
MANE Select
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NP_940890.4:p.Ala292Thr
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