ENST00000379370.7:c.1848G>T
MANE Select
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ENSP00000368678.2:p.Gly616=
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ENST00000651234.1:c.1533G>T
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ENSP00000499046.1:p.Gly511=
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ENST00000652369.1:c.1533G>T
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ENSP00000498543.1:p.Gly511=
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ENST00000379370.6:c.1848G>T
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ENSP00000368678.2:p.Gly616=
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ENST00000620552.4:c.1434G>T
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ENSP00000484607.1:p.Gly478=
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NM_001305275.1:c.1848G>T
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NP_001292204.1:p.Gly616=
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NM_198576.3:c.1848G>T
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NP_940978.2:p.Gly616=
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XM_005244749.2:c.1848G>T
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XP_005244806.1:p.Gly616=
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XM_006710635.2:c.1848G>T
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XP_006710698.1:p.Gly616=
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XM_011541429.1:c.1848G>T
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XP_011539731.1:p.Gly616=
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XM_011541430.1:c.975G>T
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XP_011539732.1:p.Gly325=
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XM_011541431.1:c.114G>T
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XP_011539733.1:p.Gly38=
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XR_946650.1:n.1915G>T
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|
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NM_001364727.1:c.1533G>T
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NP_001351656.1:p.Gly511=
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|
XM_005244749.3:c.1848G>T
|
XP_005244806.1:p.Gly616=
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|
XM_011541429.2:c.1848G>T
|
XP_011539731.1:p.Gly616=
|
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XR_946650.2:n.1919G>T
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|
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NM_001305275.2:c.1848G>T
|
NP_001292204.1:p.Gly616=
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|
NM_198576.4:c.1848G>T
MANE Select
|
NP_940978.2:p.Gly616=
|
|
NM_001364727.2:c.1533G>T
|
NP_001351656.1:p.Gly511=
|
|