ENST00000419884.6:c.156A>C
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ENST00000472420.6:n.804A>C
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ENST00000483489.2:n.156A>C
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ENST00000681993.1:n.1277A>C
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ENST00000682303.1:c.*3511A>C
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ENSP00000508325.1:n.*3511A>C
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ENST00000682308.1:c.3725A>C
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ENSP00000507056.1:p.Glu1242Ala
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ENST00000682434.1:n.1276A>C
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ENST00000682480.1:c.3743A>C
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ENSP00000508344.1:p.Glu1248Ala
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ENST00000682546.1:c.3722A>C
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ENSP00000508188.1:p.Glu1241Ala
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ENST00000682585.1:c.3725A>C
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ENSP00000506885.1:p.Glu1242Ala
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ENST00000682595.1:n.4309A>C
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ENST00000682607.1:c.2143A>C
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ENST00000682612.1:c.577A>C
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ENST00000682779.1:c.3716A>C
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ENSP00000507947.1:p.Glu1239Ala
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ENST00000682845.1:n.2827A>C
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ENST00000682885.1:c.3680A>C
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ENSP00000508036.1:p.Glu1227Ala
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ENST00000682933.1:n.3799A>C
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ENST00000683002.1:c.577A>C
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ENST00000683072.1:n.4309A>C
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ENST00000683080.1:n.1344A>C
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ENST00000683125.1:c.3833A>C
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ENSP00000507939.1:p.Glu1278Ala
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ENST00000683213.1:c.3728A>C
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ENSP00000507751.1:p.Glu1243Ala
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ENST00000683220.1:c.3755A>C
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ENSP00000507151.1:p.Glu1252Ala
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ENST00000683329.1:n.4528A>C
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ENST00000683346.1:c.*3600A>C
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ENSP00000507458.1:n.*3600A>C
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ENST00000683409.1:n.2332A>C
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ENST00000683459.1:n.4312A>C
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ENST00000683528.1:c.653A>C
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ENST00000683590.1:c.3473A>C
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ENSP00000506820.1:p.Glu1158Ala
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ENST00000683623.1:c.3632A>C
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ENSP00000507702.1:p.Glu1211Ala
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ENST00000683645.1:n.4276A>C
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ENST00000683796.1:c.*3597A>C
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ENSP00000508221.1:n.*3597A>C
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ENST00000683802.1:n.6650A>C
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ENST00000683833.1:c.3716A>C
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ENSP00000506852.1:p.Glu1239Ala
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ENST00000683994.1:c.3725A>C
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ENSP00000507181.1:p.Glu1242Ala
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ENST00000684290.1:c.*1261A>C
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ENSP00000507243.1:n.*1261A>C
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ENST00000684306.1:c.*3638A>C
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ENSP00000508384.1:n.*3638A>C
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ENST00000684341.1:n.3745A>C
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ENST00000684383.1:c.*3363A>C
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ENSP00000506863.1:n.*3363A>C
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ENST00000684418.1:n.4906A>C
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ENST00000684433.1:n.109A>C
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ENST00000684454.1:n.3075A>C
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ENST00000684619.1:c.*3597A>C
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ENSP00000508088.1:n.*3597A>C
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ENST00000684743.1:n.6470A>C
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ENST00000260665.12:c.3725A>C
MANE Select
|
ENSP00000260665.7:p.Glu1242Ala
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ENST00000260665.11:c.3725A>C
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ENSP00000260665.7:p.Glu1242Ala
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ENST00000463456.5:n.2768A>C
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ENST00000472420.5:n.122A>C
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ENST00000483489.1:n.199A>C
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NM_133259.3:c.3725A>C
|
NP_573566.2:p.Glu1242Ala
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XM_006711915.2:c.3647A>C
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XP_006711978.1:p.Glu1216Ala
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XM_011532473.1:c.3725A>C
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XP_011530775.1:p.Glu1242Ala
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XM_011532474.1:c.3725A>C
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XP_011530776.1:p.Glu1242Ala
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XM_017003117.1:c.3647A>C
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XP_016858606.1:p.Glu1216Ala
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XR_002958896.1:n.3767A>C
|
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NM_133259.4:c.3725A>C
MANE Select
|
NP_573566.2:p.Glu1242Ala
|
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