ENST00000330377.3:c.457G>T
MANE Select
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ENSP00000329312.2:p.Gly153Cys
|
|
ENST00000249053.3:c.*86G>T
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ENSP00000249053.3:n.*86G>T
|
|
ENST00000330377.2:c.457G>T
|
ENSP00000329312.2:p.Gly153Cys
|
|
ENST00000438703.1:c.460G>T
|
ENSP00000403391.1:p.Gly154Cys
|
|
NM_020070.3:c.457G>T
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NP_064455.1:p.Gly153Cys
|
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NM_152855.2:c.*86G>T
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NP_690594.1:n.*86G>T
|
|
XM_011530169.1:c.460G>T
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XP_011528471.1:p.Gly154Cys
|
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XM_011530169.2:c.460G>T
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XP_011528471.1:p.Gly154Cys
|
|
NM_020070.4:c.457G>T
MANE Select
|
NP_064455.1:p.Gly153Cys
|
|
NM_001369906.1:c.460G>T
|
NP_001356835.1:p.Gly154Cys
|
|
NM_152855.3:c.*86G>T
|
NP_690594.1:n.*86G>T
|
|