ENST00000377833.10:c.7167C>G
MANE Select
|
ENSP00000367064.4:p.Gly2389=
|
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ENST00000377833.8:c.7167C>G
|
ENSP00000367064.4:p.Gly2389=
|
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NM_001081.3:c.7167C>G , LRG_540t1:c.7167C>G
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NP_001072.2:p.Gly2389=
|
|
XM_011519708.1:c.7167C>G
|
XP_011518010.1:p.Gly2389=
|
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XM_011519709.1:c.3153C>G
|
XP_011518011.1:p.Gly1051=
|
|
XM_011519710.1:c.3129C>G
|
XP_011518012.1:p.Gly1043=
|
|
XM_011519711.1:c.3009C>G
|
XP_011518013.1:p.Gly1003=
|
|
XM_011519708.2:c.7167C>G
|
XP_011518010.1:p.Gly2389=
|
|
XM_011519709.2:c.3153C>G
|
XP_011518011.1:p.Gly1051=
|
|
XM_011519710.2:c.3129C>G
|
XP_011518012.1:p.Gly1043=
|
|
XM_011519711.3:c.3009C>G
|
XP_011518013.1:p.Gly1003=
|
|
NM_001081.4:c.7167C>G
MANE Select
|
NP_001072.2:p.Gly2389=
|
|