ENST00000209873.9:c.1053A>C
MANE Select
|
ENSP00000209873.4:p.Pro351=
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ENST00000546562.6:n.2117A>C
|
|
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ENST00000547238.6:n.1689A>C
|
|
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ENST00000547520.6:n.1047A>C
|
|
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ENST00000547757.2:c.102A>C
|
ENSP00000448020.2:p.Pro34=
|
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ENST00000548880.2:n.1503A>C
|
|
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ENST00000548931.6:c.573A>C
|
ENSP00000457518.1:p.Pro191=
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ENST00000549450.6:n.987A>C
|
|
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ENST00000552161.6:n.2009A>C
|
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ENST00000672797.1:n.1542A>C
|
|
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ENST00000672900.1:n.1995A>C
|
|
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ENST00000209873.8:c.1053A>C
|
ENSP00000209873.4:p.Pro351=
|
|
ENST00000394384.7:c.954A>C
|
ENSP00000377908.3:p.Pro318=
|
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ENST00000547520.5:n.757A>C
|
|
|
ENST00000548931.5:c.573A>C
|
ENSP00000457518.1:p.Pro191=
|
|
ENST00000550033.5:n.308A>C
|
|
|
ENST00000550286.5:c.681A>C
|
ENSP00000446885.1:p.Pro227=
|
|
ENST00000552876.5:n.1396A>C
|
|
|
NM_001173466.1:c.954A>C
|
NP_001166937.1:p.Pro318=
|
|
NM_015665.5:c.1053A>C
|
NP_056480.1:p.Pro351=
|
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XM_006719617.2:c.1068A>C
|
XP_006719680.1:p.Pro356=
|
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XM_006719619.2:c.*63A>C
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XP_006719682.1:n.*63A>C
|
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XM_011538777.1:c.1068A>C
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XP_011537079.1:p.Pro356=
|
|
XM_011538778.1:c.1053A>C
|
XP_011537080.1:p.Pro351=
|
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XM_011538779.1:c.969A>C
|
XP_011537081.1:p.Pro323=
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XM_011538780.1:c.954A>C
|
XP_011537082.1:p.Pro318=
|
|
XM_011538781.1:c.402A>C
|
XP_011537083.1:p.Pro134=
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XM_011538778.2:c.1053A>C
|
XP_011537080.1:p.Pro351=
|
|
XM_011538780.2:c.954A>C
|
XP_011537082.1:p.Pro318=
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|
XR_001748875.2:n.1110A>C
|
|
|
NM_015665.6:c.1053A>C
MANE Select
|
NP_056480.1:p.Pro351=
|
|
NM_001173466.2:c.954A>C
|
NP_001166937.1:p.Pro318=
|
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