ENST00000474627.8:c.617G=
MANE Select
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ENSP00000417190.2:p.Gly206=
|
|
ENST00000462733.5:c.*34G=
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ENSP00000463920.1:n.*34G=
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|
ENST00000465337.2:n.476G=
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|
|
ENST00000467560.5:n.27G=
|
|
|
ENST00000469327.5:n.527G=
|
|
|
ENST00000474627.7:c.617G=
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ENSP00000417190.2:p.Gly206=
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|
ENST00000488753.1:n.412G=
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|
|
ENST00000496852.5:n.1122G=
|
|
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ENST00000581698.1:c.49-2552G=
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|
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ENST00000584205.5:c.*33+3386G=
|
ENSP00000462899.1:n.*33+3386G=
|
|
ENST00000585101.5:c.*33+3386G=
|
ENSP00000463861.1:n.*33+3386G=
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|
NM_145691.3:c.617G=
|
NP_663729.1:p.Gly206=
|
|
XM_005256848.2:c.617G=
|
XP_005256905.1:p.Gly206=
|
|
XM_011524062.1:c.617G=
|
XP_011522364.1:p.Gly206=
|
|
XM_011524063.1:c.617G=
|
XP_011522365.1:p.Gly206=
|
|
XM_011524064.1:c.317G=
|
XP_011522366.1:p.Gly106=
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|
XM_011524065.1:c.617G=
|
XP_011522367.1:p.Gly206=
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|
XM_011524066.1:c.80G=
|
XP_011522368.1:p.Gly27=
|
|
XR_934116.1:n.1015G=
|
|
|
XM_005256848.4:c.617G=
|
XP_005256905.1:p.Gly206=
|
|
XM_011524065.2:c.617G=
|
XP_011522367.1:p.Gly206=
|
|
XM_017025302.1:c.317G=
|
XP_016880791.1:p.Gly106=
|
|
XM_017025303.1:c.317G=
|
XP_016880792.1:p.Gly106=
|
|
XR_001752677.2:n.1014G=
|
|
|
NM_145691.4:c.617G=
MANE Select
|
NP_663729.1:p.Gly206=
|
|