ENST00000460843.6:c.3043G>A
MANE Select
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ENSP00000417980.1:p.Ala1015Thr
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ENST00000636027.1:c.2929G>A
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ENSP00000489961.1:p.Ala977Thr
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ENST00000637161.1:c.2950G>A
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ENSP00000490328.1:p.Ala984Thr
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ENST00000637261.1:c.3083G>A
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ENSP00000490815.1:n.3083G>A
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ENST00000637891.1:c.937G>A
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ENSP00000490907.1:p.Ala313Thr
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ENST00000460843.5:c.3043G>A
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ENSP00000417980.1:p.Ala1015Thr
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ENST00000462942.3:c.1900G>A
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ENSP00000436107.1:p.Ala634Thr
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ENST00000486164.5:c.730G>A
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ENST00000488242.2:n.569G>A
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NM_024757.4:c.3043G>A
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NP_079033.4:p.Ala1015Thr
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XM_005266105.3:c.3034G>A
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XP_005266162.1:p.Ala1012Thr
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XM_005266110.1:c.2950G>A
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XP_005266167.1:p.Ala984Thr
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XM_006717288.2:c.3025G>A
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XP_006717351.1:p.Ala1009Thr
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XM_011519021.1:c.3052G>A
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XP_011517323.1:p.Ala1018Thr
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XM_011519022.1:c.3049G>A
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XP_011517324.1:p.Ala1017Thr
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XM_011519023.1:c.3031G>A
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XP_011517325.1:p.Ala1011Thr
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XM_011519024.1:c.2974G>A
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XP_011517326.1:p.Ala992Thr
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XM_011519025.1:c.2950G>A
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XP_011517327.1:p.Ala984Thr
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XM_011519026.1:c.2908G>A
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XP_011517328.1:p.Ala970Thr
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XM_011519029.1:c.1474G>A
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XP_011517331.1:p.Ala492Thr
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XM_011519030.1:c.826G>A
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XP_011517332.1:p.Ala276Thr
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XM_011519031.1:c.613G>A
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XP_011517333.1:p.Ala205Thr
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XM_011519032.1:c.613G>A
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XP_011517334.1:p.Ala205Thr
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XM_011519033.1:c.2887G>A
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XP_011517335.1:p.Ala963Thr
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NM_001354263.1:c.3022G>A
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NP_001341192.1:p.Ala1008Thr
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XM_005266105.5:c.3034G>A
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XP_005266162.1:p.Ala1012Thr
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XM_011519021.3:c.3052G>A
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XP_011517323.1:p.Ala1018Thr
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XM_011519022.3:c.3049G>A
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XP_011517324.1:p.Ala1017Thr
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XM_011519023.3:c.3031G>A
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XP_011517325.1:p.Ala1011Thr
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XM_011519029.3:c.1474G>A
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XP_011517331.1:p.Ala492Thr
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XM_011519030.3:c.826G>A
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XP_011517332.1:p.Ala276Thr
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XM_017015134.1:c.3028G>A
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XP_016870623.1:p.Ala1010Thr
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XM_017015136.2:c.2944G>A
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XP_016870625.1:p.Ala982Thr
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XM_017015137.1:c.2929G>A
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XP_016870626.1:p.Ala977Thr
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XM_017015138.1:c.2929G>A
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XP_016870627.1:p.Ala977Thr
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XM_024447674.1:c.2872G>A
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XP_024303442.1:p.Ala958Thr
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XM_024447675.1:c.2806G>A
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XP_024303443.1:p.Ala936Thr
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XM_024447676.1:c.2167G>A
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XP_024303444.1:p.Ala723Thr
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XM_024447677.1:c.2167G>A
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XP_024303445.1:p.Ala723Thr
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XM_024447680.1:c.2785G>A
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XP_024303448.1:p.Ala929Thr
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NM_024757.5:c.3043G>A
MANE Select
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NP_079033.4:p.Ala1015Thr
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NM_001354263.2:c.3022G>A
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NP_001341192.1:p.Ala1008Thr
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