ENST00000371117.8:c.10158T>C
MANE Select
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ENSP00000360158.3:p.Gly3386=
|
|
ENST00000371117.7:c.10158T>C
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ENSP00000360158.3:p.Gly3386=
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|
NM_138694.3:c.10158T>C
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NP_619639.3:p.Gly3386=
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|
XM_011514679.1:c.10158T>C
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XP_011512981.1:p.Gly3386=
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|
XM_011514680.1:c.10158T>C
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XP_011512982.1:p.Gly3386=
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|
XM_011514681.1:c.10029T>C
|
XP_011512983.1:p.Gly3343=
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|
XM_011514682.1:c.10020T>C
|
XP_011512984.1:p.Gly3340=
|
|
XM_011514683.1:c.9516T>C
|
XP_011512985.1:p.Gly3172=
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|
XM_011514684.1:c.9447T>C
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XP_011512986.1:p.Gly3149=
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|
XM_011514687.1:c.10157-10748T>C
|
XP_011512989.1:n.10157-10748T>C
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|
XM_011514690.1:c.4233T>C
|
XP_011512992.1:p.Gly1411=
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|
XM_011514691.1:c.4233T>C
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XP_011512993.1:p.Gly1411=
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|
XR_926870.1:n.535+7595A>G
|
|
|
XR_926871.1:n.403+7595A>G
|
|
|
XR_926872.1:n.535+7595A>G
|
|
|
XM_011514680.3:c.10158T>C
|
XP_011512982.1:p.Gly3386=
|
|
XM_011514682.3:c.10020T>C
|
XP_011512984.1:p.Gly3340=
|
|
XM_011514683.3:c.9516T>C
|
XP_011512985.1:p.Gly3172=
|
|
XM_011514684.3:c.9447T>C
|
XP_011512986.1:p.Gly3149=
|
|
XM_011514690.3:c.4233T>C
|
XP_011512992.1:p.Gly1411=
|
|
XM_011514691.3:c.4233T>C
|
XP_011512993.1:p.Gly1411=
|
|
XM_017010944.2:c.10158T>C
|
XP_016866433.1:p.Gly3386=
|
|
XM_017010945.2:c.10083T>C
|
XP_016866434.1:p.Gly3361=
|
|
XM_017010946.2:c.9963T>C
|
XP_016866435.1:p.Gly3321=
|
|
XM_017010947.2:c.9894T>C
|
XP_016866436.1:p.Gly3298=
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|
XM_017010948.2:c.9447T>C
|
XP_016866437.1:p.Gly3149=
|
|
XM_017010949.2:c.8298T>C
|
XP_016866438.1:p.Gly2766=
|
|
XR_001743469.1:n.10434T>C
|
|
|
XR_001744157.1:n.3145+7595A>G
|
|
|
XR_926870.2:n.3145+7595A>G
|
|
|
XR_926871.2:n.3013+7595A>G
|
|
|
XR_926872.2:n.3145+7595A>G
|
|
|
NM_138694.4:c.10158T>C
MANE Select
|
NP_619639.3:p.Gly3386=
|
|