ENST00000420323.7:c.3442G=
MANE Select
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ENSP00000401514.2:p.Val1148=
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ENST00000420323.6:c.3442G=
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ENSP00000401514.2:p.Val1148=
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|
ENST00000486752.5:n.3703G=
|
|
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ENST00000497875.1:n.3607G=
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|
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NM_015512.4:c.3442G=
|
NP_056327.4:p.Val1148=
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|
XM_011533577.1:c.3442G=
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XP_011531879.1:p.Val1148=
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|
XM_017006129.1:c.3442G=
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XP_016861618.1:p.Val1148=
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|
XM_017006130.1:c.3442G=
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XP_016861619.1:p.Val1148=
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|
XM_017006131.1:c.3442G=
|
XP_016861620.1:p.Val1148=
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|
XM_017006132.1:c.3442G=
|
XP_016861621.1:p.Val1148=
|
|
XM_017006133.1:c.3442G=
|
XP_016861622.1:p.Val1148=
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XR_001740098.1:n.6591G=
|
|
|
XR_001740099.1:n.6591G=
|
|
|
NM_015512.5:c.3442G=
MANE Select
|
NP_056327.4:p.Val1148=
|
|