ENST00000681993.1:n.498A=
|
|
|
ENST00000682295.1:c.210A=
|
ENSP00000507499.1:p.Gln70=
|
|
ENST00000682303.1:c.*2732A=
|
ENSP00000508325.1:n.*2732A=
|
|
ENST00000682308.1:c.2946A=
|
ENSP00000507056.1:p.Gln982=
|
|
ENST00000682480.1:c.2946A=
|
ENSP00000508344.1:p.Gln982=
|
|
ENST00000682546.1:c.2943A=
|
ENSP00000508188.1:p.Gln981=
|
|
ENST00000682585.1:c.2946A=
|
ENSP00000506885.1:p.Gln982=
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ENST00000682595.1:n.3530A=
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|
ENST00000682607.1:c.1364A=
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ENST00000682779.1:c.2937A=
|
ENSP00000507947.1:p.Gln979=
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|
ENST00000682845.1:n.2048A=
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|
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ENST00000682885.1:c.2901A=
|
ENSP00000508036.1:p.Gln967=
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ENST00000682933.1:n.3020A=
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ENST00000683072.1:n.3530A=
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ENST00000683080.1:n.565A=
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ENST00000683125.1:c.3054A=
|
ENSP00000507939.1:p.Gln1018=
|
|
ENST00000683213.1:c.2949A=
|
ENSP00000507751.1:p.Gln983=
|
|
ENST00000683220.1:c.2976A=
|
ENSP00000507151.1:p.Gln992=
|
|
ENST00000683236.1:c.276A=
|
ENSP00000506891.1:n.276A=
|
|
ENST00000683329.1:n.3749A=
|
|
|
ENST00000683346.1:c.*2821A=
|
ENSP00000507458.1:n.*2821A=
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ENST00000683409.1:n.1553A=
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ENST00000683459.1:n.3533A=
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ENST00000683590.1:c.2897-5791A=
|
ENSP00000506820.1:n.2897-5791A=
|
|
ENST00000683623.1:c.2853A=
|
ENSP00000507702.1:p.Gln951=
|
|
ENST00000683645.1:n.3497A=
|
|
|
ENST00000683796.1:c.*2818A=
|
ENSP00000508221.1:n.*2818A=
|
|
ENST00000683802.1:n.5871A=
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|
ENST00000683833.1:c.2937A=
|
ENSP00000506852.1:p.Gln979=
|
|
ENST00000683994.1:c.2946A=
|
ENSP00000507181.1:p.Gln982=
|
|
ENST00000684290.1:c.*482A=
|
ENSP00000507243.1:n.*482A=
|
|
ENST00000684306.1:c.*2859A=
|
ENSP00000508384.1:n.*2859A=
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ENST00000684341.1:n.2966A=
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ENST00000684383.1:c.*2584A=
|
ENSP00000506863.1:n.*2584A=
|
|
ENST00000684619.1:c.*2818A=
|
ENSP00000508088.1:n.*2818A=
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ENST00000684705.1:n.67A=
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ENST00000684743.1:n.3977A=
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ENST00000260665.12:c.2946A=
MANE Select
|
ENSP00000260665.7:p.Gln982=
|
|
ENST00000260665.11:c.2946A=
|
ENSP00000260665.7:p.Gln982=
|
|
NM_133259.3:c.2946A=
|
NP_573566.2:p.Gln982=
|
|
XM_006711915.2:c.2868A=
|
XP_006711978.1:p.Gln956=
|
|
XM_006711916.2:c.2946A=
|
XP_006711979.1:p.Gln982=
|
|
XM_011532473.1:c.2946A=
|
XP_011530775.1:p.Gln982=
|
|
XM_011532474.1:c.2946A=
|
XP_011530776.1:p.Gln982=
|
|
XM_006711916.3:c.2946A=
|
XP_006711979.1:p.Gln982=
|
|
XM_017003117.1:c.2868A=
|
XP_016858606.1:p.Gln956=
|
|
XR_002958896.1:n.2988A=
|
|
|
NM_133259.4:c.2946A=
MANE Select
|
NP_573566.2:p.Gln982=
|
|