ENST00000456935.7:c.162A=
MANE Select
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ENSP00000395473.2:p.Thr54=
|
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ENST00000221363.8:c.162A=
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ENSP00000221363.4:p.Thr54=
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|
ENST00000456935.6:c.162A=
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ENSP00000395473.2:p.Thr54=
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ENST00000466794.5:n.144A=
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|
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ENST00000486847.2:c.160-278A=
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ENSP00000470174.1:n.160-278A=
|
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ENST00000596512.5:n.201-278A=
|
|
|
ENST00000597961.1:c.153A=
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ENSP00000472710.1:p.Thr51=
|
|
ENST00000598876.1:c.189A=
|
ENSP00000470533.1:p.Thr63=
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ENST00000600281.1:n.203A=
|
|
|
NM_000528.3:c.162A=
|
NP_000519.2:p.Thr54=
|
|
NM_001173498.1:c.162A=
|
NP_001166969.1:p.Thr54=
|
|
XM_005259913.1:c.162A=
|
XP_005259970.1:p.Thr54=
|
|
XM_005259913.2:c.162A=
|
XP_005259970.1:p.Thr54=
|
|
XM_024451518.1:c.-857A=
|
XP_024307286.1:n.-857A=
|
|
NM_000528.4:c.162A=
MANE Select
|
NP_000519.2:p.Thr54=
|
|
NM_001173498.2:c.162A=
|
NP_001166969.1:p.Thr54=
|
|