ENST00000346342.8:c.832A>C
MANE Select
|
ENSP00000329546.4:p.Asn278His
|
|
ENST00000346342.7:c.832A>C
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ENSP00000329546.3:p.Asn278His
|
|
ENST00000375581.3:c.898A>C
|
ENSP00000364731.3:p.Asn300His
|
|
ENST00000541084.5:c.646A>C
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ENSP00000442051.2:p.Asn216His
|
|
NM_000131.4:c.898A>C , LRG_554t1:c.898A>C
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NP_000122.1:p.Asn300His
|
|
NM_001267554.1:c.646A>C
|
NP_001254483.1:p.Asn216His
|
|
NM_019616.3:c.832A>C , LRG_554t2:c.832A>C
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NP_062562.1:p.Asn278His
|
|
NR_051961.1:n.919A>C
|
|
|
XM_006719963.2:c.691A>C
|
XP_006720026.1:p.Asn231His
|
|
XM_011537474.1:c.940A>C
|
XP_011535776.1:p.Asn314His
|
|
XM_011537475.1:c.754A>C
|
XP_011535777.1:p.Asn252His
|
|
XM_011537476.1:c.592A>C
|
XP_011535778.1:p.Asn198His
|
|
XM_011537477.1:c.901A>C
|
XP_011535779.1:p.Asn301His
|
|
XM_006719963.3:c.736A>C
|
XP_006720026.2:p.Asn246His
|
|
XM_011537474.2:c.985A>C
|
XP_011535776.2:p.Asn329His
|
|
XM_011537475.2:c.799A>C
|
XP_011535777.2:p.Asn267His
|
|
XM_011537476.2:c.592A>C
|
XP_011535778.1:p.Asn198His
|
|
NM_019616.4:c.832A>C
MANE Select
|
NP_062562.1:p.Asn278His
|
|
NR_051961.2:n.916A>C
|
|
|
NM_001267554.2:c.646A>C
|
NP_001254483.1:p.Asn216His
|
|