ENST00000706989.1:c.2642G>C
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ENSP00000516702.1:p.Gly881Ala
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ENST00000359125.7:c.2588G>C
MANE Select
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ENSP00000352035.2:p.Gly863Ala
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ENST00000637193.1:c.1985G>C
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ENSP00000490734.1:p.Gly662Ala
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ENST00000344462.8:c.2495G>C
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ENSP00000339611.4:p.Gly832Ala
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ENST00000357249.6:c.2156G>C
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ENSP00000349789.3:p.Gly719Ala
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ENST00000359125.6:c.2588G>C
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ENSP00000352035.2:p.Gly863Ala
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ENST00000360480.7:c.2504G>C
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ENSP00000353668.3:p.Gly835Ala
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ENST00000370224.5:c.2241+371G>C
|
ENSP00000359244.2:n.2241+371G>C
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ENST00000625514.2:c.2205+371G>C
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ENSP00000486040.1:n.2205+371G>C
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ENST00000626839.2:c.2534G>C
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ENSP00000486706.1:p.Gly845Ala
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ENST00000629241.2:c.2133+371G>C
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ENSP00000487142.1:n.2133+371G>C
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ENST00000629676.2:c.1680-5832G>C
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ENSP00000486194.1:n.1680-5832G>C
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NM_004518.4:c.2504G>C
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NP_004509.2:p.Gly835Ala
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NM_172106.1:c.2534G>C
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NP_742104.1:p.Gly845Ala
|
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NM_172107.2:c.2588G>C
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NP_742105.1:p.Gly863Ala
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NM_172108.3:c.2495G>C
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NP_742106.1:p.Gly832Ala
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XM_006723787.1:c.2630G>C
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XP_006723850.1:p.Gly877Ala
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XM_011528807.1:c.2696G>C
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XP_011527109.1:p.Gly899Ala
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XM_011528808.1:c.2693G>C
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XP_011527110.1:p.Gly898Ala
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XM_011528809.1:c.2666G>C
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XP_011527111.1:p.Gly889Ala
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XM_011528810.1:c.2642G>C
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XP_011527112.1:p.Gly881Ala
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XM_011528811.1:c.2612G>C
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XP_011527113.1:p.Gly871Ala
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XM_011528812.1:c.2585G>C
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XP_011527114.1:p.Gly862Ala
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XM_011528813.1:c.2570G>C
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XP_011527115.1:p.Gly857Ala
|
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XM_011528814.1:c.2177G>C
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XP_011527116.1:p.Gly726Ala
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NM_004518.5:c.2504G>C
|
NP_004509.2:p.Gly835Ala
|
|
NM_172106.2:c.2534G>C
|
NP_742104.1:p.Gly845Ala
|
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NM_172107.3:c.2588G>C
|
NP_742105.1:p.Gly863Ala
|
|
NM_172108.4:c.2495G>C
|
NP_742106.1:p.Gly832Ala
|
|
XM_011528810.2:c.2642G>C
|
XP_011527112.1:p.Gly881Ala
|
|
XM_011528811.2:c.2612G>C
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XP_011527113.1:p.Gly871Ala
|
|
XM_017027841.2:c.2639G>C
|
XP_016883330.1:p.Gly880Ala
|
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XM_017027842.2:c.2576G>C
|
XP_016883331.1:p.Gly859Ala
|
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XM_017027843.1:c.2573G>C
|
XP_016883332.1:p.Gly858Ala
|
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XM_017027844.2:c.2531G>C
|
XP_016883333.1:p.Gly844Ala
|
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XM_017027845.1:c.1604G>C
|
XP_016883334.1:p.Gly535Ala
|
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NM_004518.6:c.2504G>C
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NP_004509.2:p.Gly835Ala
|
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NM_172106.3:c.2534G>C
|
NP_742104.1:p.Gly845Ala
|
|
NM_172107.4:c.2588G>C
MANE Select
|
NP_742105.1:p.Gly863Ala
|
|
NM_172108.5:c.2495G>C
|
NP_742106.1:p.Gly832Ala
|
|
NM_001382235.1:c.2642G>C
|
NP_001369164.1:p.Gly881Ala
|
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