ENST00000334504.12:c.4841G=
MANE Select
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ENSP00000334733.7:p.Gly1614=
|
|
ENST00000334504.11:c.4841G=
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ENSP00000334733.7:p.Gly1614=
|
|
ENST00000372216.8:c.4844G=
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ENSP00000361290.4:p.Gly1615=
|
|
ENST00000394872.6:c.4892G=
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ENSP00000378340.3:p.Gly1631=
|
|
ENST00000538570.5:c.4670G=
|
ENSP00000445236.1:p.Gly1557=
|
|
ENST00000545689.2:c.4805G=
|
ENSP00000443707.2:p.Gly1602=
|
|
ENST00000621266.4:c.4769G=
|
ENSP00000482970.1:p.Gly1590=
|
|
NM_001287758.1:c.4892G=
|
NP_001274687.1:p.Gly1631=
|
|
NM_001287759.1:c.4769G=
|
NP_001274688.1:p.Gly1590=
|
|
NM_001287760.1:c.4670G=
|
NP_001274689.1:p.Gly1557=
|
|
NM_001847.3:c.4844G=
|
NP_001838.2:p.Gly1615=
|
|
NM_033641.3:c.4841G=
|
NP_378667.1:p.Gly1614=
|
|
XM_006724617.2:c.4895G=
|
XP_006724680.1:p.Gly1632=
|
|
XM_011530852.1:c.4823G=
|
XP_011529154.1:p.Gly1608=
|
|
XM_011530853.1:c.4811G=
|
XP_011529155.1:p.Gly1604=
|
|
XM_006724617.3:c.4895G=
|
XP_006724680.1:p.Gly1632=
|
|
XM_011530852.2:c.4823G=
|
XP_011529154.1:p.Gly1608=
|
|
XM_011530853.3:c.4811G=
|
XP_011529155.1:p.Gly1604=
|
|
NM_001847.4:c.4844G=
|
NP_001838.2:p.Gly1615=
|
|
NM_033641.4:c.4841G=
MANE Select
|
NP_378667.1:p.Gly1614=
|
|
NM_001287758.2:c.4892G=
|
NP_001274687.1:p.Gly1631=
|
|
NM_001287759.2:c.4769G=
|
NP_001274688.1:p.Gly1590=
|
|
NM_001287760.2:c.4670G=
|
NP_001274689.1:p.Gly1557=
|
|