ENST00000379370.7:c.4894G=
MANE Select
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ENSP00000368678.2:p.Gly1632=
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ENST00000651234.1:c.4579G=
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ENSP00000499046.1:p.Gly1527=
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ENST00000652369.1:c.4579G=
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ENSP00000498543.1:p.Gly1527=
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ENST00000379370.6:c.4894G=
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ENSP00000368678.2:p.Gly1632=
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ENST00000620552.4:c.4480G=
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ENSP00000484607.1:p.Gly1494=
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NM_001305275.1:c.4894G=
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NP_001292204.1:p.Gly1632=
|
|
NM_198576.3:c.4894G=
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NP_940978.2:p.Gly1632=
|
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XM_005244749.2:c.4894G=
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XP_005244806.1:p.Gly1632=
|
|
XM_006710635.2:c.4894G=
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XP_006710698.1:p.Gly1632=
|
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XM_011541429.1:c.4894G=
|
XP_011539731.1:p.Gly1632=
|
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XM_011541430.1:c.4021G=
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XP_011539732.1:p.Gly1341=
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XM_011541431.1:c.3160G=
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XP_011539733.1:p.Gly1054=
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XR_946650.1:n.4961G=
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|
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NM_001364727.1:c.4579G=
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NP_001351656.1:p.Gly1527=
|
|
XM_005244749.3:c.4894G=
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XP_005244806.1:p.Gly1632=
|
|
XM_011541429.2:c.4894G=
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XP_011539731.1:p.Gly1632=
|
|
XR_946650.2:n.4965G=
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|
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NM_001305275.2:c.4894G=
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NP_001292204.1:p.Gly1632=
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|
NM_198576.4:c.4894G=
MANE Select
|
NP_940978.2:p.Gly1632=
|
|
NM_001364727.2:c.4579G=
|
NP_001351656.1:p.Gly1527=
|
|