ENST00000266771.10:c.576G>A
MANE Select
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ENSP00000266771.5:p.Arg192=
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|
ENST00000266771.9:c.576G>A
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ENSP00000266771.5:p.Arg192=
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|
ENST00000366292.6:n.888G>A
|
|
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ENST00000376740.8:c.155G>A
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ENST00000376744.8:c.412G>A
|
|
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ENST00000535272.1:n.370G>A
|
|
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ENST00000539703.1:n.226G>A
|
|
|
NM_145648.3:c.576G>A
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NP_663623.1:p.Arg192=
|
|
XM_011537895.1:c.726G>A
|
XP_011536197.1:p.Arg242=
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XR_429081.2:n.599G>A
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XR_944494.1:n.749G>A
|
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XR_944495.1:n.749G>A
|
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XR_944496.1:n.749G>A
|
|
|
XR_944497.1:n.749G>A
|
|
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XM_017018791.1:c.726G>A
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XP_016874280.1:p.Arg242=
|
|
XM_017018792.1:c.726G>A
|
XP_016874281.1:p.Arg242=
|
|
XM_017018793.1:c.576G>A
|
XP_016874282.1:p.Arg192=
|
|
XR_002957287.1:n.599G>A
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|
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XR_944496.2:n.749G>A
|
|
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NM_145648.4:c.576G>A
MANE Select
|
NP_663623.1:p.Arg192=
|
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