ENST00000371117.8:c.11167G>C
MANE Select
|
ENSP00000360158.3:p.Gly3723Arg
|
|
ENST00000371117.7:c.11167G>C
|
ENSP00000360158.3:p.Gly3723Arg
|
|
NM_138694.3:c.11167G>C
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NP_619639.3:p.Gly3723Arg
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XM_011514679.1:c.11167G>C
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XP_011512981.1:p.Gly3723Arg
|
|
XM_011514680.1:c.11167G>C
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XP_011512982.1:p.Gly3723Arg
|
|
XM_011514681.1:c.11038G>C
|
XP_011512983.1:p.Gly3680Arg
|
|
XM_011514682.1:c.11029G>C
|
XP_011512984.1:p.Gly3677Arg
|
|
XM_011514683.1:c.10525G>C
|
XP_011512985.1:p.Gly3509Arg
|
|
XM_011514684.1:c.10456G>C
|
XP_011512986.1:p.Gly3486Arg
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XM_011514687.1:c.10157-9739G>C
|
XP_011512989.1:n.10157-9739G>C
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|
XM_011514690.1:c.5242G>C
|
XP_011512992.1:p.Gly1748Arg
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|
XM_011514691.1:c.5242G>C
|
XP_011512993.1:p.Gly1748Arg
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XR_926870.1:n.535+6586C>G
|
|
|
XR_926871.1:n.403+6586C>G
|
|
|
XR_926872.1:n.535+6586C>G
|
|
|
XM_011514680.3:c.11167G>C
|
XP_011512982.1:p.Gly3723Arg
|
|
XM_011514682.3:c.11029G>C
|
XP_011512984.1:p.Gly3677Arg
|
|
XM_011514683.3:c.10525G>C
|
XP_011512985.1:p.Gly3509Arg
|
|
XM_011514684.3:c.10456G>C
|
XP_011512986.1:p.Gly3486Arg
|
|
XM_011514690.3:c.5242G>C
|
XP_011512992.1:p.Gly1748Arg
|
|
XM_011514691.3:c.5242G>C
|
XP_011512993.1:p.Gly1748Arg
|
|
XM_017010944.2:c.11167G>C
|
XP_016866433.1:p.Gly3723Arg
|
|
XM_017010945.2:c.11092G>C
|
XP_016866434.1:p.Gly3698Arg
|
|
XM_017010946.2:c.10972G>C
|
XP_016866435.1:p.Gly3658Arg
|
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XM_017010947.2:c.10903G>C
|
XP_016866436.1:p.Gly3635Arg
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XM_017010948.2:c.10456G>C
|
XP_016866437.1:p.Gly3486Arg
|
|
XM_017010949.2:c.9307G>C
|
XP_016866438.1:p.Gly3103Arg
|
|
XR_001743469.1:n.11443G>C
|
|
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XR_001744157.1:n.3145+6586C>G
|
|
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XR_926870.2:n.3145+6586C>G
|
|
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XR_926871.2:n.3013+6586C>G
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|
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XR_926872.2:n.3145+6586C>G
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|
|
NM_138694.4:c.11167G>C
MANE Select
|
NP_619639.3:p.Gly3723Arg
|
|