ENST00000700061.1:c.4319G=
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ENST00000700062.1:c.4426+13550G=
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ENST00000700063.1:c.844G=
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|
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ENST00000700064.1:c.2189G=
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|
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ENST00000281513.10:c.6333G=
MANE Select
|
ENSP00000281513.5:p.Gln2111=
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ENST00000281513.9:c.6333G=
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ENSP00000281513.5:p.Gln2111=
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|
ENST00000417461.5:c.512+13550G=
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ENSP00000392421.1:n.512+13550G=
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ENST00000442506.5:c.3476G=
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NM_015909.3:c.6333G=
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NP_056993.2:p.Gln2111=
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|
NR_052013.2:n.6280+13550G=
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XM_011510357.1:c.6204G=
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XP_011508659.1:p.Gln2068=
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|
XM_011510358.1:c.6333G=
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XP_011508660.1:p.Gln2111=
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XM_011510359.1:c.5694G=
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XP_011508661.1:p.Gln1898=
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XM_011510360.1:c.4134G=
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XP_011508662.1:p.Gln1378=
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XM_011510361.1:c.4125G=
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XP_011508663.1:p.Gln1375=
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|
XM_011510357.2:c.6204G=
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XP_011508659.1:p.Gln2068=
|
|
XM_011510358.2:c.6333G=
|
XP_011508660.1:p.Gln2111=
|
|
XM_011510360.2:c.4134G=
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XP_011508662.1:p.Gln1378=
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|
XM_011510361.2:c.4125G=
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XP_011508663.1:p.Gln1375=
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|
XM_017004317.1:c.6333G=
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XP_016859806.1:p.Gln2111=
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|
XM_024452961.1:c.5694G=
|
XP_024308729.1:p.Gln1898=
|
|
NM_015909.4:c.6333G=
MANE Select
|
NP_056993.2:p.Gln2111=
|
|
NR_052013.3:n.6266+13550G=
|
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