ENST00000394329.9:c.12669G>A
MANE Select
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ENSP00000377862.4:p.Gln4223=
|
|
ENST00000674496.2:c.7440G>A
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ENSP00000501473.2:p.Gln2480=
|
|
ENST00000335110.5:c.7386G>A
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ENSP00000335169.5:p.Gln2462=
|
|
ENST00000394329.7:c.12663G>A
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ENSP00000377862.3:p.Gln4221=
|
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NM_001291285.1:c.12669G>A
|
NP_001278214.1:p.Gln4223=
|
|
NM_001291303.1:c.12669G>A
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NP_001278232.1:p.Gln4223=
|
|
NM_024582.4:c.12663G>A
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NP_078858.4:p.Gln4221=
|
|
XM_011532236.1:c.12669G>A
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XP_011530538.1:p.Gln4223=
|
|
XM_011532237.1:c.7440G>A
|
XP_011530539.1:p.Gln2480=
|
|
XM_011532236.2:c.12669G>A
|
XP_011530538.1:p.Gln4223=
|
|
XM_011532237.2:c.7440G>A
|
XP_011530539.1:p.Gln2480=
|
|
NM_001291285.2:c.12669G>A
|
NP_001278214.1:p.Gln4223=
|
|
NM_001291303.3:c.12669G>A
MANE Select
|
NP_001278232.1:p.Gln4223=
|
|
NM_024582.5:c.12663G>A
|
NP_078858.4:p.Gln4221=
|
|
NM_001291285.3:c.12669G>A
|
NP_001278214.1:p.Gln4223=
|
|
NM_024582.6:c.12663G>A
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NP_078858.4:p.Gln4221=
|
|