ENST00000346342.8:c.762C>A
MANE Select
|
ENSP00000329546.4:p.His254Gln
|
|
ENST00000346342.7:c.762C>A
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ENSP00000329546.3:p.His254Gln
|
|
ENST00000375581.3:c.828C>A
|
ENSP00000364731.3:p.His276Gln
|
|
ENST00000541084.5:c.576C>A
|
ENSP00000442051.2:p.His192Gln
|
|
NM_000131.4:c.828C>A , LRG_554t1:c.828C>A
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NP_000122.1:p.His276Gln
|
|
NM_001267554.1:c.576C>A
|
NP_001254483.1:p.His192Gln
|
|
NM_019616.3:c.762C>A , LRG_554t2:c.762C>A
|
NP_062562.1:p.His254Gln
|
|
NR_051961.1:n.849C>A
|
|
|
XM_006719963.2:c.621C>A
|
XP_006720026.1:p.His207Gln
|
|
XM_011537474.1:c.870C>A
|
XP_011535776.1:p.His290Gln
|
|
XM_011537475.1:c.684C>A
|
XP_011535777.1:p.His228Gln
|
|
XM_011537476.1:c.522C>A
|
XP_011535778.1:p.His174Gln
|
|
XM_011537477.1:c.831C>A
|
XP_011535779.1:p.His277Gln
|
|
XM_006719963.3:c.666C>A
|
XP_006720026.2:p.His222Gln
|
|
XM_011537474.2:c.915C>A
|
XP_011535776.2:p.His305Gln
|
|
XM_011537475.2:c.729C>A
|
XP_011535777.2:p.His243Gln
|
|
XM_011537476.2:c.522C>A
|
XP_011535778.1:p.His174Gln
|
|
NM_019616.4:c.762C>A
MANE Select
|
NP_062562.1:p.His254Gln
|
|
NR_051961.2:n.846C>A
|
|
|
NM_001267554.2:c.576C>A
|
NP_001254483.1:p.His192Gln
|
|