ENST00000266771.10:c.792G>A
MANE Select
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ENSP00000266771.5:p.Leu264=
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ENST00000266771.9:c.792G>A
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ENSP00000266771.5:p.Leu264=
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|
ENST00000366292.6:n.1104G>A
|
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ENST00000376740.8:c.371G>A
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ENST00000376744.8:c.628G>A
|
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ENST00000539703.1:n.442G>A
|
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ENST00000614634.1:c.-51G>A
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ENSP00000483143.1:n.-51G>A
|
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NM_145648.3:c.792G>A
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NP_663623.1:p.Leu264=
|
|
XM_011537895.1:c.942G>A
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XP_011536197.1:p.Leu314=
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XR_429081.2:n.815G>A
|
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XR_944494.1:n.965G>A
|
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XR_944495.1:n.965G>A
|
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XR_944496.1:n.965G>A
|
|
|
XR_944497.1:n.965G>A
|
|
|
XM_017018791.1:c.942G>A
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XP_016874280.1:p.Leu314=
|
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XM_017018792.1:c.942G>A
|
XP_016874281.1:p.Leu314=
|
|
XM_017018793.1:c.792G>A
|
XP_016874282.1:p.Leu264=
|
|
XR_002957287.1:n.815G>A
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XR_944496.2:n.965G>A
|
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|
NM_145648.4:c.792G>A
MANE Select
|
NP_663623.1:p.Leu264=
|
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