ENST00000324856.13:c.5256G>C
MANE Select
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ENSP00000320485.7:p.Lys1752Asn
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ENST00000374152.7:c.4107G>C
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ENSP00000363267.2:p.Lys1369Asn
|
|
ENST00000430799.7:c.4104G>C
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ENSP00000390317.3:p.Lys1368Asn
|
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ENST00000466382.2:c.673G>C
|
|
|
ENST00000636219.1:c.4110G>C
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ENSP00000489842.1:p.Lys1370Asn
|
|
ENST00000637788.1:n.1056G>C
|
|
|
ENST00000324856.11:c.5256G>C
|
ENSP00000320485.7:p.Lys1752Asn
|
|
ENST00000374152.6:c.4107G>C
|
ENSP00000363267.2:p.Lys1369Asn
|
|
ENST00000430799.6:c.1945G>C
|
|
|
ENST00000457599.6:c.4605G>C
|
ENSP00000387636.2:p.Lys1535Asn
|
|
ENST00000466382.1:c.673G>C
|
|
|
ENST00000532781.1:c.754G>C
|
|
|
NM_006015.4:c.5256G>C , LRG_875t1:c.5256G>C
|
NP_006006.3:p.Lys1752Asn
|
|
NM_139135.2:c.4605G>C
|
NP_624361.1:p.Lys1535Asn
|
|
NM_006015.5:c.5256G>C
|
NP_006006.3:p.Lys1752Asn
|
|
NM_139135.3:c.4605G>C
|
NP_624361.1:p.Lys1535Asn
|
|
NM_006015.6:c.5256G>C
MANE Select
|
NP_006006.3:p.Lys1752Asn
|
|
NM_139135.4:c.4605G>C
|
NP_624361.1:p.Lys1535Asn
|
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