ENST00000682114.1:c.542A=
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ENSP00000507245.1:p.Tyr181=
|
|
ENST00000682478.1:n.732A=
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|
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ENST00000683576.1:n.732A=
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|
|
ENST00000683627.1:c.542A=
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ENSP00000507533.1:p.Tyr181=
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|
ENST00000684082.1:c.499A=
|
ENSP00000508266.1:n.499A=
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ENST00000684633.1:n.514A=
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|
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ENST00000684678.1:c.538A=
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ENSP00000507059.1:n.538A=
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|
ENST00000369842.9:c.542A=
MANE Select
|
ENSP00000358857.4:p.Tyr181=
|
|
ENST00000369835.3:c.437A=
|
ENSP00000358850.3:p.Tyr146=
|
|
ENST00000369842.8:c.542A=
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ENSP00000358857.4:p.Tyr181=
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|
ENST00000428228.5:c.*447A=
|
ENSP00000401081.1:n.*447A=
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|
ENST00000471965.1:n.331A=
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|
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ENST00000486738.5:n.979A=
|
|
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ENST00000492448.1:n.525A=
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|
|
NM_000117.2:c.542A= , LRG_745t1:c.542A=
|
NP_000108.1:p.Tyr181=
|
|
XM_024452349.1:c.548A=
|
XP_024308117.1:p.Tyr183=
|
|
NM_000117.3:c.542A=
MANE Select
|
NP_000108.1:p.Tyr181=
|
|