ENST00000377873.8:c.810G>C
MANE Select
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ENSP00000367104.3:p.Gln270His
|
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ENST00000536626.7:c.393G>C
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ENSP00000442522.1:p.Gln131His
|
|
ENST00000377868.6:c.435G>C
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ENSP00000367099.2:p.Gln145His
|
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ENST00000377873.7:c.810G>C
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ENSP00000367104.3:p.Gln270His
|
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ENST00000536626.5:c.393G>C
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ENSP00000442522.1:p.Gln131His
|
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NM_001161705.1:c.435G>C
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NP_001155177.1:p.Gln145His
|
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NM_001195.4:c.810G>C
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NP_001186.1:p.Gln270His
|
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NM_001278606.1:c.393G>C
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NP_001265535.1:p.Gln131His
|
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NM_001278607.1:c.477G>C
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NP_001265536.1:p.Gln159His
|
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NM_001278608.1:c.393G>C
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NP_001265537.1:p.Gln131His
|
|
XM_011529312.1:c.393G>C
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XP_011527614.1:p.Gln131His
|
|
XM_017028005.2:c.702G>C
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XP_016883494.1:p.Gln234His
|
|
NM_001195.5:c.810G>C
MANE Select
|
NP_001186.1:p.Gln270His
|
|
NM_001161705.2:c.435G>C
|
NP_001155177.1:p.Gln145His
|
|
NM_001278606.2:c.393G>C
|
NP_001265535.1:p.Gln131His
|
|
NM_001278607.2:c.477G>C
|
NP_001265536.1:p.Gln159His
|
|
NM_001278608.2:c.393G>C
|
NP_001265537.1:p.Gln131His
|
|